Ichthyosis

Harlequin Ichthyosis
By: Dan Hood, Matt Sharbaugh, Brian Monterroso
http://academics.hamilton.edu

Diagnosis of X-Linked Recessive Ichthyosis
http://comenius.susqu.edu

Genodermatoses and Acquired Syndromes
Rick Lin, DO MPH
http://www.atsu.edu

Genodermatoses and Acquired Syndromes,
Adam Wray, D.O
http://www.atsu.edu/

Ichthyosis vulgaris
Julia Akaah M.D.
http://www.med.wayne.edu

Atopic Dermatitis
Nnenna G. Agim, MD
http://www.bcm.edu

X-Linked Ichthyosis
http://www.med.unc.edu/

Neonatal Dermatology
Mikelle Key-Solle MD
http://pediatrics.med.unc.edu/

Dermatology and Systemic Medical Associations
Johnnie M. Woodson, M.D.
http://www.medicine.nevada.edu

Matters of Sex, Multifactorial Traits & Behavior
http://www.canyons.edu

Genodermatosis
http://www.atsu.edu

Epidermal Nevi, Neoplasms and Cysts
JoAnne M. LaRow, D.O.
http://www.atsu.edu

279 free full text published articles
 1. Pallagatti S, Sheikh S, Kaur A, Aggarwal A, Singh R. X-linked ichthyosis along with epidermolysis bullosa. Contemp Clin Dent. 2012 Apr;3(Suppl 1).S96-8.
 2. Li H, Törmä H. Retinoids Reduce Formation of Keratin Aggregates in Heat-stressed Immortalized Keratinocytes from an Epidermolytic Ichthyosis Patient with a KRT10 Mutation*. Acta Derm Venereol. 2012 Apr 16. doi. 10.2340/00015555-1368. [Epub ahead of print]
 3. Tokuriki A, Kiyohara T, Ido T, Kumakiri M. A Case of Lymphomatoid Papulosis with Extensive Limb Disease Followed by Extracutaneous Involvement and Acquired Ichthyosis. Acta Derm Venereol. 2012 Jun 8;92(3).278-279. doi. 10.2340/00015555-1314.
 4. Carrascosa-Romero MC, Suela J, Alfaro-Ponce B, Cepillo-Boluda AJ. [X-chromosome-linked ichthyosis associated to epilepsy, hyperactivity, autism and mental retardation, due to the Xp22.31 microdeletion]. Rev Neurol. 2012 Feb 16;54(4).241-8. Review. Spanish.
 5. Gånemo A, Sommerlund M, Vahlquist A. Oral Alitretinoin in Congenital Ichthyosis. A Pilot Study Shows Variable Effects and a Risk of Central Hypothyroidism. Acta Derm Venereol. 2012 Jun 8;92(3).256-257. doi. 10.2340/00015555-1302.
 6. Winge MC, Hoppe T, Berne B, Vahlquist A, Nordenskjöld M, Bradley M, Törmä H. Filaggrin genotype determines functional and molecular alterations in skin of patients with atopic dermatitis and ichthyosis vulgaris. PLoS One. 2011;6(12).e28254. Epub 2011 Dec 2.
 7. Aldahmesh MA, Mohamed JY, Alkuraya HS, Verma IC, Puri RD, Alaiya AA, Rizzo WB, Alkuraya FS. Recessive mutations in ELOVL4 cause ichthyosis, intellectual disability, and spastic quadriplegia. Am J Hum Genet. 2011 Dec 9;89(6).745-50. Epub 2011 Nov 17.
 8. Mese G, Sellitto C, Li L, Wang HZ, Valiunas V, Richard G, Brink PR, White TW.  The Cx26-G45E mutation displays increased hemichannel activity in a mouse model of the lethal form of keratitis-ichthyosis-deafness syndrome. Mol Biol Cell. 2011 Dec;22(24).4776-86. Epub 2011 Oct 26.
 9. Blaydon DC, Nitoiu D, Eckl KM, Cabral RM, Bland P, Hausser I, van Heel DA, Rajpopat S, Fischer J, Oji V, Zvulunov A, Traupe H, Hennies HC, Kelsell DP. Mutations in CSTA, encoding Cystatin A, underlie exfoliative ichthyosis and reveal a role for this protease inhibitor in cell-cell adhesion. Am J Hum Genet.  2011 Oct 7;89(4).564-71. doi. 10.1016/j.ajhg.2011.09.001. Epub 2011 Sep 22.
 10. Ozgur OR, Akcay L, Tutas N, Ozkurt Y. Cicatricial upper and lower eyelid ectropion in an ichthyosis patient. Surgical correction. J Dermatol Case Rep. 2011 Jun 6;5(2).27-9.
 11. Alshami M, Bawazir MA, Atwan AA. Photoletter to the editor. A new variant of  ichthyosis follicularis with alopecia and photophobia (IFAP) syndrome with coexisting psoriasiform lesions and palmoplantar keratoderma. IFAP-PPK syndrome?  J Dermatol Case Rep. 2011 Mar 26;5(1).14-6.
 12. Li Q, Frank M, Akiyama M, Shimizu H, Ho SY, Thisse C, Thisse B, Sprecher E, Uitto J. Abca12-mediated lipid transport and Snap29-dependent trafficking of lamellar granules are crucial for epidermal morphogenesis in a zebrafish model of ichthyosis. Dis Model Mech. 2011 Nov;4(6).777-85. Epub 2011 Aug 4.
 13. Kim EJ, Jeong MS, Li K, Park MK, Lee MK, Yoon Y, Cho DY, Seo SJ. Genetic Polymorphism of FLG in Korean Ichthyosis Vulgaris Patients. Ann Dermatol. 2011 May;23(2).170-6. Epub 2011 May 27.
 14. Chakraborti C, Tripathi P, Bandopadhyay G, Mazumder DB. Congenital bilateral  ectropion in lamellar ichthyosis. Oman J Ophthalmol. 2011 Jan;4(1).35-6.
 15. Höpker LM, Ribeiro CG, Oliveira LM, Moreira AT. Ichthyosis follicularis, alopecia and photophobia syndrome (IFAP). report of the first case with ocular and cutaneous manifestations in Brazil with a favorable response to treatment. Arq Bras Oftalmol. 2011 Jan-Feb;74(1).55-7.
 16. Mégarbané H, Mégarbané A. Ichthyosis follicularis, alopecia, and photophobia  (IFAP) syndrome. Orphanet J Rare Dis. 2011 May 21;6.29. Review.
 17. Gruber R, Elias PM, Crumrine D, Lin TK, Brandner JM, Hachem JP, Presland RB,  Fleckman P, Janecke AR, Sandilands A, McLean WH, Fritsch PO, Mildner M, Tschachler E, Schmuth M. Filaggrin genotype in ichthyosis vulgaris predicts abnormalities in epidermal structure and function. Am J Pathol. 2011 May;178(5).2252-63.
 18. Hazuku T, Yamada K, Imaizumi M, Ikebe T, Shinoda K, Nakatsuka K, Sekiguchi K, Izumi T, Nishida Y. Unusual protrusion of conjunctiva in two neonates with harlequin ichthyosis. Case Report Ophthalmol. 2011 Feb 21;2(1).73-7.
 19. Sobol M, Dahl N, Klar J. FATP4 missense and nonsense mutations cause similar  features in Ichthyosis Prematurity Syndrome. BMC Res Notes. 2011 Mar 30;4.90.
 20. Israeli S, Khamaysi Z, Fuchs-Telem D, Nousbeck J, Bergman R, Sarig O, Sprecher E. A mutation in LIPN, encoding epidermal lipase N, causes a late-onset  form of autosomal-recessive congenital ichthyosis. Am J Hum Genet. 2011 Apr 8;88(4).482-7.
 21. Frateschi S, Camerer E, Crisante G, Rieser S, Membrez M, Charles RP, Beermann F, Stehle JC, Breiden B, Sandhoff K, Rotman S, Haftek M, Wilson A, Ryser S, Steinhoff M, Coughlin SR, Hummler E. PAR2 absence completely rescues inflammation and ichthyosis caused by altered CAP1/Prss8 expression in mouse skin. Nat Commun. 2011 Jan 18;2.161.
 22. Milstone LM, Rizzo WB, Pickford JR. Meeting report from Frontiers in Ichthyosis Research. J Invest Dermatol. 2011 Feb;131(2).279-82.
 23. Yu X, Espinoza-Lewis RA, Sun C, Lin L, He F, Xiong W, Yang J, Wang A, Chen Y. Overexpression of constitutively active BMP-receptor-IB in mouse skin causes an ichthyosis-vulgaris-like disease. Cell Tissue Res. 2010 Dec;342(3).401-10. Epub 2010 Nov 16.
 24. Mrabet D, Rekik S, Khiari H, Sahli H, Azaiez O, Cheour I, Elleuch M, Mnif E,  Mokni M, Meddeb N, Sellami S. [An unusual association. rheumatoid arthritis associated with vascularitis myositis and ichthyosis]. Tunis Med. 2010 Nov;88(11).856-7. French.
 25. Schütz M, Auth T, Gehrt A, Bosen F, Körber I, Strenzke N, Moser T, Willecke K. The connexin26 S17F mouse mutant represents a model for the human hereditary keratitis-ichthyosis-deafness syndrome. Hum Mol Genet. 2011 Jan 1;20(1).28-39. Epub 2010 Oct 6.
 26. Vahlquist A. Pleomorphic ichthyosis. proposed name for a heterogeneous group  of congenital ichthyoses with phenotypic shifting and mild residual scaling. Acta Derm Venereol. 2010 Sep;90(5).454-60. Review.
 27. Traupe H. In this issue. Rapid categorization of mild types of autosomal recessive congenital ichthyosis undergoing a phenotypic shift. should it be called "pleomorphic ichthyosis" or "congenital ichthyosis with mild scaling (CIMS)"? Acta Derm Venereol. 2010 Sep;90(5).450-3.
 28. Taïeb A, Morice-Picard F. In this issue. Comments on the proposed term pleomorphic ichthyosis. Acta Derm Venereol. 2010 Sep;90(5).450-3.
 29. Choate KA, Lu Y, Zhou J, Choi M, Elias PM, Farhi A, Nelson-Williams C, Crumrine D, Williams ML, Nopper AJ, Bree A, Milstone LM, Lifton RP. Mitotic recombination in patients with ichthyosis causes reversion of dominant mutations  in KRT10. Science. 2010 Oct 1;330(6000).94-7. Epub 2010 Aug 26.
 30. Bellew S, Del Rosso JQ. Overcoming the Barrier Treatment of Ichthyosis. A Combination-therapy Approach. J Clin Aesthet Dermatol. 2010 Jul;3(7).49-53.
 31. Preumont A, Rzem R, Vertommen D, Van Schaftingen E. HDHD1, which is often deleted in X-linked ichthyosis, encodes a pseudouridine-5'-phosphatase. Biochem J. 2010 Oct 15;431(2).237-44.
 32. Jiang H, Jans R, Xu W, Rorke EA, Lin CY, Chen YW, Fang S, Zhong Y, Eckert RL. Type I transglutaminase accumulation in the endoplasmic reticulum may be an underlying cause of autosomal recessive congenital ichthyosis. J Biol Chem. 2010  Oct 8;285(41).31634-46. Epub 2010 Jul 27.
 33. Wang WH, Song SJ, Li LF, Zhang L, Yang SM, Zhang Q, Wang YY, Sun TT. Disturbed keratin expression and distinct genotype of ichthyosis hystrix Lambert  type. Eur J Dermatol. 2010 Sep-Oct;20(5).567-72. Epub 2010 Jul 7.
 34. Sánchez HA, Mese G, Srinivas M, White TW, Verselis VK. Differentially altered Ca2+ regulation and Ca2+ permeability in Cx26 hemichannels formed by the A40V and G45E mutations that cause keratitis ichthyosis deafness syndrome. J Gen Physiol.  2010 Jul;136(1).47-62.
 35. Trindade F, Fiadeiro T, Torrelo A, Hennies HC, Hausser I, Traupe H. Bathing suit ichthyosis. Eur J Dermatol. 2010 Jul-Aug;20(4).447-50. Epub 2010 Jun 3. Review.
 36. Yanagi T, Akiyama M, Nishihara H, Ishikawa J, Sakai K, Miyamura Y, Naoe A, Kitahara T, Tanaka S, Shimizu H. Self-improvement of keratinocyte differentiation defects during skin maturation in ABCA12-deficient harlequin ichthyosis model mice. Am J Pathol. 2010 Jul;177(1).106-18. Epub 2010 May 20.
 37. O'Shaughnessy RF, Choudhary I, Harper JI. Interleukin-1 alpha blockade prevents hyperkeratosis in an in vitro model of lamellar ichthyosis. Hum Mol Genet. 2010 Jul 1;19(13).2594-605. Epub 2010 Apr 12.
 38. Richard G, Bale SJ. Autosomal Recessive Congenital Ichthyosis . 2001 Jan 10 [updated 2012 Apr 19]. In. Pagon RA, Bird TD, Dolan CR, Stephens K, Adam MP, editors. GeneReviews™ [Internet]. Seattle (WA). University of Washington, Seattle; 1993-. Available from http.//www.ncbi.nlm.nih.gov/books/NBK1420/
 39. Akiyama M, Sakai K, Yanagi T, Fukushima S, Ihn H, Hitomi K, Shimizu H. Transglutaminase1 preferred substrate peptide K5 is an efficient tool in diagnosis of lamellar ichthyosis. Am J Pathol. 2010 Apr;176(4).1592-9. Epub 2010  Feb 18.
 40. Rizzo WB, S'Aulis D, Jennings MA, Crumrine DA, Williams ML, Elias PM. Ichthyosis in Sjögren-Larsson syndrome reflects defective barrier function due to abnormal lamellar body structure and secretion. Arch Dermatol Res. 2010 Aug;302(6).443-51. Epub 2010 Jan 5.
 41. Sanli H, Akay BN, Sen BB, Kocak AY, Emral R, Bostanci S. Acquired ichthyosis  associated with type 1 diabetes mellitus. Dermatoendocrinol. 2009 Jan;1(1).34-6.
 42. Wajid M, Kurban M, Shimomura Y, Christiano AM. NIPAL4/ichthyin is expressed in the granular layer of human epidermis and mutated in two Pakistani families with autosomal recessive ichthyosis. Dermatology. 2010;220(1).8-14. Epub 2009 Dec 10.
 43. Turgut B, Aydemir O, Kaya M, Türkçüoğlu P, Demir T, Celiker U. Spontaneous corneal perforation in a patient with lamellar ichthyosis and dry eye. Clin Ophthalmol. 2009;3.611-3. Epub 2009 Nov 16.
 44. Gonzalez ME, Tlougan BE, Price HN, Patel R, Kamino H, Schaffer JV. Keratitis-ichthyosis-deafness (KID) syndrome. Dermatol Online J. 2009 Aug 15;15(8).11.
 45. Vahlquist A, Bygum A, Gånemo A, Virtanen M, Hellström-Pigg M, Strauss G, Brandrup F, Fischer J. Genotypic and clinical spectrum of self-improving collodion ichthyosis. ALOX12B, ALOXE3, and TGM1 mutations in Scandinavian patients. J Invest Dermatol. 2010 Feb;130(2).438-43. Epub 2009 Nov 5.
 46. Klar J, Schweiger M, Zimmerman R, Zechner R, Li H, Törmä H, Vahlquist A, Bouadjar B, Dahl N, Fischer J. Mutations in the fatty acid transport protein 4 gene cause the ichthyosis prematurity syndrome. Am J Hum Genet. 2009 Aug;85(2).248-53. Epub 2009 Jul 23.
 47. Djalilian AR, Kim JY, Saeed HN, Holland EJ, Chan CC. Histopathology and treatment of corneal disease in keratitis, ichthyosis, and deafness (KID) syndrome. Eye (Lond). 2010 Apr;24(4).738-40. Epub 2009 Jul 10.
 48. Fischer J. Autosomal recessive congenital ichthyosis. J Invest Dermatol. 2009 Jun;129(6).1319-21.
 49. Levy O, Tishler M. Acquired ichthyosis as the primary manifestation of renal  cell carcinoma. Isr Med Assoc J. 2009 Feb;11(2).121-2.
 50. Szabo R, Kosa P, List K, Bugge TH. Loss of matriptase suppression underlies spint1 mutation-associated ichthyosis and postnatal lethality. Am J Pathol. 2009  Jun;174(6).2015-22. Epub 2009 Apr 23.
 51. Herman ML, Farasat S, Steinbach PJ, Wei MH, Toure O, Fleckman P, Blake P, Bale SJ, Toro JR. Transglutaminase-1 gene mutations in autosomal recessive congenital ichthyosis. summary of mutations (including 23 novel) and modeling of  TGase-1. Hum Mutat. 2009 Apr;30(4).537-47. Review.
 52. Aufenvenne K, Oji V, Walker T, Becker-Pauly C, Hennies HC, Stöcker W, Traupe  H. Transglutaminase-1 and bathing suit ichthyosis. molecular analysis of gene/environment interactions. J Invest Dermatol. 2009 Aug;129(8).2068-71. Epub 2009 Feb 12.
 53. Pavez Loriè E, Gånemo A, Borgers M, Wouters L, Blockhuys S, van de Plassche L, Törmä H, Vahlquist A. Expression of retinoid-regulated genes in lamellar ichthyosis vs. healthy control epidermis. changes after oral treatment with liarozole. Acta Derm Venereol. 2009;89(1).12-20.
 54. Thomas AC, Tattersall D, Norgett EE, O'Toole EA, Kelsell DP. Premature terminal differentiation and a reduction in specific proteases associated with loss of ABCA12 in Harlequin ichthyosis. Am J Pathol. 2009 Mar;174(3).970-8. Epub  2009 Jan 29.
 55. Eckl KM, de Juanes S, Kurtenbach J, Nätebus M, Lugassy J, Oji V, Traupe H, Preil ML, Martínez F, Smolle J, Harel A, Krieg P, Sprecher E, Hennies HC. Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis. evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B. J Invest Dermatol. 2009 Jun;129(6).1421-8. Epub 2009 Jan 8.
 56. Nomura T, Akiyama M, Sandilands A, Nemoto-Hasebe I, Sakai K, Nagasaki A, Palmer CN, Smith FJ, McLean WH, Shimizu H. Prevalent and rare mutations in the gene encoding filaggrin in Japanese patients with ichthyosis vulgaris and atopic  dermatitis. J Invest Dermatol. 2009 May;129(5).1302-5. Epub 2008 Nov 27.
 57. Farasat S, Wei MH, Herman M, Liewehr DJ, Steinberg SM, Bale SJ, Fleckman P, Toro JR. Novel transglutaminase-1 mutations and genotype-phenotype investigations of 104 patients with autosomal recessive congenital ichthyosis in the USA. J Med  Genet. 2009 Feb;46(2).103-11. Epub 2008 Oct 23.
 58. Alef T, Torres S, Hausser I, Metze D, Türsen U, Lestringant GG, Hennies HC. Ichthyosis, follicular atrophoderma, and hypotrichosis caused by mutations in ST14 is associated with impaired profilaggrin processing. J Invest Dermatol. 2009 Apr;129(4).862-9. Epub 2008 Oct 9.
 59. Titeux M, Mendonça V, Décha A, Moreira E, Magina S, Maia A, Lacaze-Buzy L, Mejía JE, Torrão L, Carvalho F, Eça-Guimarães J, Hovnanian A. Keratitis-ichthyosis-deafness syndrome caused by GJB2 maternal mosaicism. J Invest Dermatol. 2009 Mar;129(3).776-9. Epub 2008 Oct 9.
 60. Nagaike K, Kawaguchi M, Takeda N, Fukushima T, Sawaguchi A, Kohama K, Setoyama M, Kataoka H. Defect of hepatocyte growth factor activator inhibitor type 1/serine protease inhibitor, Kunitz type 1 (Hai-1/Spint1) leads to ichthyosis-like condition and abnormal hair development in mice. Am J Pathol. 2008 Nov;173(5).1464-75. Epub 2008 Oct 2.
 61. Smyth I, Hacking DF, Hilton AA, Mukhamedova N, Meikle PJ, Ellis S, Satterley  K, Collinge JE, de Graaf CA, Bahlo M, Sviridov D, Kile BT, Hilton DJ. A mouse model of harlequin ichthyosis delineates a key role for Abca12 in lipid homeostasis. PLoS Genet. 2008 Sep 19;4(9).e1000192. Erratum in. PLoS Genet. 2008  Oct;4(10). doi. 10.1371/annotation/02a793a0-160f-46b9-abaa-4a3d3eecdde2. Slattery, Keith [corrected to Satterley, Keith].
 62. Nemoto-Hasebe I, Akiyama M, Yamada N, Inoue Y, Touge C, Shimizu H. Keratitis-ichthyosis-deafness syndrome lacking subjective hearing impairment. Acta Derm Venereol. 2008;88(4).406-8.
 63. Yanagi T, Akiyama M, Nishihara H, Sakai K, Nishie W, Tanaka S, Shimizu H. Harlequin ichthyosis model mouse reveals alveolar collapse and severe fetal skin  barrier defects. Hum Mol Genet. 2008 Oct 1;17(19).3075-83. Epub 2008 Jul 15.
 64. Ross R, DiGiovanna JJ, Capaldi L, Argenyi Z, Fleckman P, Robinson-Bostom L. Histopathologic characterization of epidermolytic hyperkeratosis. a systematic review of histology from the National Registry for Ichthyosis and Related Skin Disorders. J Am Acad Dermatol. 2008 Jul;59(1).86-90. Review.
 65. Mauldin EA, Credille KM, Dunstan RW, Casal ML. The clinical and morphologic features of nonepidermolytic ichthyosis in the golden retriever. Vet Pathol. 2008 Mar;45(2).174-80.
 66. Désilets A, Béliveau F, Vandal G, McDuff FO, Lavigne P, Leduc R. Mutation G827R in matriptase causing autosomal recessive ichthyosis with hypotrichosis yields an inactive protease. J Biol Chem. 2008 Apr 18;283(16).10535-42. Epub 2008 Feb 8.
 67. Chen H, Ho JC, Sandilands A, Chan YC, Giam YC, Evans AT, Lane EB, McLean WH.  Unique and recurrent mutations in the filaggrin gene in Singaporean Chinese patients with ichthyosis vulgaris. J Invest Dermatol. 2008 Jul;128(7).1669-75. Epub 2008 Jan 31. Erratum in. J Invest Dermatol. 2008 Oct;128(10).2545.
 68. Murhekar K, Majhi U, Sridevi V, Rajkumar T. Does "ichthyosis uteri" have malignant potential? A case report of squamous cell carcinoma of endometrium associated with extensive ichthyosis uteri. Diagn Pathol. 2008 Jan 31;3.4.
 69. Nomura T, Akiyama M, Sandilands A, Nemoto-Hasebe I, Sakai K, Nagasaki A, Ota  M, Hata H, Evans AT, Palmer CN, Shimizu H, McLean WH. Specific filaggrin mutations cause ichthyosis vulgaris and are significantly associated with atopic  dermatitis in Japan. J Invest Dermatol. 2008 Jun;128(6).1436-41. Epub 2008 Jan 17.
 70. Vahlquist A, Gånemo A, Virtanen M. Congenital ichthyosis. an overview of current and emerging therapies. Acta Derm Venereol. 2008;88(1).4-14. Review.
 71. Dardano S, Gandolfi B, Parma P, Polli M, Bighignoli B, Strillacci MG, Cozzi MC, Molteni L, Longeri M. Characterization of bovine TGM1 and exclusion as candidate gene for ichthyosis in Chianina. J Hered. 2008 Jan-Feb;99(1).81-3. Epub 2007 Dec 28.
 72. Schmuth M, Gruber R, Elias PM, Williams ML. Ichthyosis update. towards a function-driven model of pathogenesis of the disorders of cornification and the role of corneocyte proteins in these disorders. Adv Dermatol. 2007;23.231-56. Review.
 73. Liu P, Yang Q, Wang X, Feng A, Yang T, Yang R, Wang P, Yuang M, Liu M, Liu JY, Wang QK. Identification of a genetic locus for ichthyosis vulgaris on chromosome 10q22.3-q24.2. J Invest Dermatol. 2008 Jun;128(6).1418-22. Epub 2007 Dec 13.
 74. Hamada T, Sandilands A, Fukuda S, Sakaguchi S, Ohyama B, Yasumoto S, McLean WH, Hashimoto T. De novo occurrence of the filaggrin mutation p.R501X with prevalent mutation c.3321delA in a Japanese family with ichthyosis vulgaris complicated by atopic dermatitis. J Invest Dermatol. 2008 May;128(5).1323-5. Epub 2007 Nov 15.
 75. List K, Currie B, Scharschmidt TC, Szabo R, Shireman J, Molinolo A, Cravatt BF, Segre J, Bugge TH. Autosomal ichthyosis with hypotrichosis syndrome displays  low matriptase proteolytic activity and is phenocopied in ST14 hypomorphic mice.  J Biol Chem. 2007 Dec 14;282(50).36714-23. Epub 2007 Oct 16.
 76. Sathish Kumar T, Scott XJ, Simon A, Raghupathy P. Vitamin D deficiency rickets with Lamellar ichthyosis. J Postgrad Med. 2007 Jul-Sep;53(3).215-7.
 77. Wenghoefer M, Allam JP, Novak N, Maintz L, Martini M, Bergé S. Surgical therapy in a patient with Keratosis-Ichthyosis-Deafness (KID) syndrome associated with follicular occlusion triad. Eur J Dermatol. 2007 Sep-Oct;17(5).449-50. Epub  2007 Aug 2.
 78. Phadnis SV, Griffin DR, Eady RA, Rodeck CH, Chitty LS. Prenatal diagnosis and management strategies in a family with a rare type of congenital ichthyosis. Ultrasound Obstet Gynecol. 2007 Nov;30(6).908-10. Review.
 79. Liao H, Waters AJ, Goudie DR, Aitken DA, Graham G, Smith FJ, Lewis-Jones S, McLean WH. Filaggrin mutations are genetic modifying factors exacerbating X-linked ichthyosis. J Invest Dermatol. 2007 Dec;127(12).2795-8. Epub 2007 Jul 26.
 80. Hu ZM, Xie ZG, Wu LQ, Liang DS, Zhu HY, Pan Q, Long ZG, Dai HP, Xia JH, Xia K. [Mapping of pathogenic genes in a pedigree with autosomal dominant ichthyosis  vulgaris]. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2007 Jun;29(3).302-6. Chinese.
 81. Fischer J, Negre-Salvayre A, Salvayre R. [Neutral lipid storage diseases and  ATGL (adipose triglyceride lipase) and CGI-58/ABHD5 (alpha-beta hydrolase domain-containing 5) deficiency. myopathy, ichthyosis, but no obesity]. Med Sci (Paris). 2007 Jun-Jul;23(6-7).575-8. French.
 82. Dahlqvist J, Klar J, Hausser I, Anton-Lamprecht I, Pigg MH, Gedde-Dahl T Jr,  Gånemo A, Vahlquist A, Dahl N. Congenital ichthyosis. mutations in ichthyin are associated with specific structural abnormalities in the granular layer of epidermis. J Med Genet. 2007 Oct;44(10).615-20. Epub 2007 Jun 8.
 83. Cho JK, Son JM, Lee DS, Park SJ, Cho SW, Shin ST. Harlequin ichthyosis in a HanWoo calf. J Vet Med Sci. 2007 May;69(5).553-5.
 84. Krishnamurthy S, Kapoor S, Yadav S. Nephrotic syndrome with X-linked ichthyosis, Kallmann Syndrome and unilateral renal agenesis. Indian Pediatr. 2007 Apr;44(4).301-3.
 85. Rabhi M, Ennibi K, Harket A, Al Bouzidi A, Labraimi A, Chaari J, Toloune F. Acquired ichthyosis disclosing non-Hodgkin's malignant lymphoma. Intern Med. 2007;46(7).397-9. Epub 2007 Apr 2.
 86. Wassif CA, Brownson KE, Sterner AL, Forlino A, Zerfas PM, Wilson WK, Starost  MF, Porter FD. HEM dysplasia and ichthyosis are likely laminopathies and not due  to 3beta-hydroxysterol Delta14-reductase deficiency. Hum Mol Genet. 2007 May 15;16(10).1176-87. Epub 2007 Apr 2.
 87. Basel-Vanagaite L, Attia R, Ishida-Yamamoto A, Rainshtein L, Ben Amitai D, Lurie R, Pasmanik-Chor M, Indelman M, Zvulunov A, Saban S, Magal N, Sprecher E, Shohat M. Autosomal recessive ichthyosis with hypotrichosis caused by a mutation  in ST14, encoding type II transmembrane serine protease matriptase. Am J Hum Genet. 2007 Mar;80(3).467-77. Epub 2007 Jan 23.
 88. Bianchi L, Papoutsaki M, Orlandi A, Citarella L, Chimenti S. Ichthyosiform mycosis fungoides. a neoplastic acquired ichthyosis. Acta Derm Venereol. 2007;87(1).82-3.
 89. Gruber R, Janecke AR, Fauth C, Utermann G, Fritsch PO, Schmuth M. Filaggrin mutations p.R501X and c.2282del4 in ichthyosis vulgaris. Eur J Hum Genet. 2007 Feb;15(2).179-84. Epub 2006 Dec 13.
 90. Lesueur F, Bouadjar B, Lefèvre C, Jobard F, Audebert S, Lakhdar H, Martin L,  Tadini G, Karaduman A, Emre S, Saker S, Lathrop M, Fischer J. Novel mutations in  ALOX12B in patients with autosomal recessive congenital ichthyosis and evidence for genetic heterogeneity on chromosome 17p13. J Invest Dermatol. 2007 Apr;127(4).829-34. Epub 2006 Nov 30.
 91. Akiyama M, Titeux M, Sakai K, McMillan JR, Tonasso L, Calvas P, Jossic F, Hovnanian A, Shimizu H. DNA-based prenatal diagnosis of harlequin ichthyosis and  characterization of ABCA12 mutation consequences. J Invest Dermatol. 2007 Mar;127(3).568-73. Epub 2006 Nov 2.
 92. Arita K, Jacyk WK, Wessagowit V, van Rensburg EJ, Chaplin T, Mein CA, Akiyama M, Shimizu H, Happle R, McGrath JA. The South African "bathing suit ichthyosis" is a form of lamellar ichthyosis caused by a homozygous missense mutation, p.R315L, in transglutaminase 1. J Invest Dermatol. 2007 Feb;127(2).490-3. Epub 2006 Sep 14.
 93. Oji V, Hautier JM, Ahvazi B, Hausser I, Aufenvenne K, Walker T, Seller N, Steijlen PM, Küster W, Hovnanian A, Hennies HC, Traupe H. Bathing suit ichthyosis is caused by transglutaminase-1 deficiency. evidence for a temperature-sensitive  phenotype. Hum Mol Genet. 2006 Nov 1;15(21).3083-97. Epub 2006 Sep 12.
 94. Thomas AC, Cullup T, Norgett EE, Hill T, Barton S, Dale BA, Sprecher E, Sheridan E, Taylor AE, Wilroy RS, DeLozier C, Burrows N, Goodyear H, Fleckman P,  Stephens KG, Mehta L, Watson RM, Graham R, Wolf R, Slavotinek A, Martin M, Bourn  D, Mein CA, O'Toole EA, Kelsell DP. ABCA12 is the major harlequin ichthyosis gene. J Invest Dermatol. 2006 Nov;126(11).2408-13. Epub 2006 Aug 10.
 95. Griffith AJ, Yang Y, Pryor SP, Park HJ, Jabs EW, Nadol JB Jr, Russell LJ, Wasserman DI, Richard G, Adams JC, Merchant SN. Cochleosaccular dysplasia associated with a connexin 26 mutation in keratitis-ichthyosis-deafness syndrome. Laryngoscope. 2006 Aug;116(8).1404-8.
 96. Arita K, Akiyama M, Aizawa T, Umetsu Y, Segawa I, Goto M, Sawamura D, Demura  M, Kawano K, Shimizu H. A novel N14Y mutation in Connexin26 in keratitis-ichthyosis-deafness syndrome. analyses of altered gap junctional communication and molecular structure of N terminus of mutated Connexin26. Am J Pathol. 2006 Aug;169(2).416-23.
 97. Sandilands A, O'Regan GM, Liao H, Zhao Y, Terron-Kwiatkowski A, Watson RM, Cassidy AJ, Goudie DR, Smith FJ, McLean WH, Irvine AD. Prevalent and rare mutations in the gene encoding filaggrin cause ichthyosis vulgaris and predispose individuals to atopic dermatitis. J Invest Dermatol. 2006 Aug;126(8).1770-5. Epub 2006 Jun 29.
 98. Fadare O. Dysplastic Ichthyosis uteri-like changes of the entire endometrium  associated with a squamous cell carcinoma of the uterine cervix. Diagn Pathol. 2006 May 19;1.8.
 99. Demerjian M, Crumrine DA, Milstone LM, Williams ML, Elias PM. Barrier dysfunction and pathogenesis of neutral lipid storage disease with ichthyosis (Chanarin-Dorfman syndrome). J Invest Dermatol. 2006 Sep;126(9).2032-8. Epub 2006 Jun 1.
 100. Rai VM, Shenoi SD. Ichthyosis follicularis with alopecia and photophobia (IFAP) syndrome. Indian J Dermatol Venereol Leprol. 2006 Mar-Apr;72(2).136-8.
 101. Segre JA. Epidermal differentiation complex yields a secret. mutations in the cornification protein filaggrin underlie ichthyosis vulgaris. J Invest Dermatol. 2006 Jun;126(6).1202-4.
 102. Akiyama M, Sakai K, Sugiyama-Nakagiri Y, Yamanaka Y, McMillan JR, Sawamura D, Niizeki H, Miyagawa S, Shimizu H. Compound heterozygous mutations including a  de novo missense mutation in ABCA12 led to a case of harlequin ichthyosis with moderate clinical severity. J Invest Dermatol. 2006 Jul;126(7).1518-23. Epub 2006 May 4.
 103. Gonzalez-Huerta LM, Messina-Baas OM, Toral-Lopez J, Rivera-Vega MR, Kofman-Alfaro S, Cuevas-Covarrubias SA. Point mutation in the STS gene in a severely affected patient with X-linked recessive ichthyosis. Acta Derm Venereol. 2006;86(1).78-9.
 104. Rajiv S, Rakhesh SV. Ichthyosis bullosa of Siemens. response to topical tazarotene. Indian J Dermatol Venereol Leprol. 2006 Jan-Feb;72(1).43-6.
 105. Lefèvre C, Bouadjar B, Ferrand V, Tadini G, Mégarbané A, Lathrop M, Prud'homme JF, Fischer J. Mutations in a new cytochrome P450 gene in lamellar ichthyosis type 3. Hum Mol Genet. 2006 Mar 1;15(5).767-76. Epub 2006 Jan 25.
 106. Richardson ES, Lee JB, Hyde PH, Richard G. A novel mutation and large size polymorphism affecting the V2 domain of keratin 1 in an African-American family with severe, diffuse palmoplantar keratoderma of the ichthyosis hystrix Curth-Macklin type. J Invest Dermatol. 2006 Jan;126(1).79-84.
 107. Rai VM, Shenoi SD. Ichthyosis follicularis with congenital atrichia, nail dystrophy and palmoplantar keratoderma. Variant of IFAP syndrome or a new entity? Dermatol Online J. 2005 Dec 1;11(3).36.
 108. Victor F, Schaffer JV. Lamellar ichthyosis. Dermatol Online J. 2005 Dec 30;11(4).13.
 109. Hazan C, Orlow SJ, Schaffer JV. X-linked recessive ichthyosis. Dermatol Online J. 2005 Dec 30;11(4).12.
 110. Hou JW. Detection of gene deletions in children with chondrodysplasia punctata, ichthyosis, Kallmann syndrome, and ocular albinism by FISH studies. Chang Gung Med J. 2005 Sep;28(9).643-50.
 111. Jacyk WK. Bathing-suit ichthyosis. A peculiar phenotype of lamellar ichthyosis in South African blacks. Eur J Dermatol. 2005 Nov-Dec;15(6).433-6.
 112. Cotellessa C, Cuevas-Covarrubias SA, Valeri P, Fargnoli MC, Peris K. Topical tazarotene 0.05% versus glycolic acid 70% treatment in X-linked ichthyosis due to extensive deletion of the STS gene. Acta Derm Venereol. 2005;85(4).346-8.
 113. Maintz L, Betz RC, Allam JP, Wenzel J, Jaksche A, Friedrichs N, Bieber T, Novak N. Keratitis-ichthyosis-deafness syndrome in association with follicular occlusion triad. Eur J Dermatol. 2005 Sep-Oct;15(5).347-52.
 114. Mizrachi-Koren M, Geiger D, Indelman M, Bitterman-Deutsch O, Bergman R, Sprecher E. Identification of a novel locus associated with congenital recessive  ichthyosis on 12p11.2-q13. J Invest Dermatol. 2005 Sep;125(3).456-62.
 115. Liu A, Xiao SX, Tan SS, Jiao T, Liu Y, Li XL, Zhou SN. [Investigation of steroid sulfatase gene in two pedigrees with X-linked ichthyosis]. Di Yi Jun Yi Da Xue Xue Bao. 2005 Aug;25(8).1023-5. Chinese.
 116. Akiyama M, Sugiyama-Nakagiri Y, Sakai K, McMillan JR, Goto M, Arita K, Tsuji-Abe Y, Tabata N, Matsuoka K, Sasaki R, Sawamura D, Shimizu H. Mutations in  lipid transporter ABCA12 in harlequin ichthyosis and functional recovery by corrective gene transfer. J Clin Invest. 2005 Jul;115(7).1777-84.
 117. Hovnanian A. Harlequin ichthyosis unmasked. a defect of lipid transport. J Clin Invest. 2005 Jul;115(7).1708-10. Review.
 118. Gicquel JJ, Vabres P, Dighiero P. [Use of topical cutaneous N-acetylcysteine in the treatment of major bilateral ectropion in an infant with lamellar ichthyosis]. J Fr Ophtalmol. 2005 Apr;28(4).412-5. French.
 119. Sprecher E, Ishida-Yamamoto A, Mizrahi-Koren M, Rapaport D, Goldsher D, Indelman M, Topaz O, Chefetz I, Keren H, O'brien TJ, Bercovich D, Shalev S, Geiger D, Bergman R, Horowitz M, Mandel H. A mutation in SNAP29, coding for a SNARE protein involved in intracellular trafficking, causes a novel neurocutaneous syndrome characterized by cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma. Am J Hum Genet. 2005 Aug;77(2).242-51.  Epub 2005 Jun 20.
 120. Nadir E, Yerman S, Feldman M. A female neonate with Hirschsprung's disease and ichthyosis. Isr Med Assoc J. 2005 May;7(5).342-3.
 121. Van Esch H, Hollanders K, Badisco L, Melotte C, Van Hummelen P, Vermeesch JR, Devriendt K, Fryns JP, Marynen P, Froyen G. Deletion of VCX-A due to NAHR plays a major role in the occurrence of mental retardation in patients with X-linked ichthyosis. Hum Mol Genet. 2005 Jul 1;14(13).1795-803. Epub 2005 May 11.
 122. Tsolia M, Aroni K, Konstantopoulou I, Karpathios T, Tsoukatou T, Paraskevakou H, Stavrinadis C, Fretzayas A. Ichthyosis follicularis with alopecia and photophobia in a girl with cataract. histological and electron microscopy findings. Acta Derm Venereol. 2005;85(1).51-5.
 123. Kelsell DP, Norgett EE, Unsworth H, Teh MT, Cullup T, Mein CA, Dopping-Hepenstal PJ, Dale BA, Tadini G, Fleckman P, Stephens KG, Sybert VP, Mallory SB, North BV, Witt DR, Sprecher E, Taylor AE, Ilchyshyn A, Kennedy CT, Goodyear H, Moss C, Paige D, Harper JI, Young BD, Leigh IM, Eady RA, O'Toole EA.  Mutations in ABCA12 underlie the severe congenital skin disease harlequin ichthyosis. Am J Hum Genet. 2005 May;76(5).794-803. Epub 2005 Mar 8.
 124. Hewett DR, Simons AL, Mangan NE, Jolin HE, Green SM, Fallon PG, McKenzie AN. Lethal, neonatal ichthyosis with increased proteolytic processing of filaggrin in a mouse model of Netherton syndrome. Hum Mol Genet. 2005 Jan 15;14(2).335-46. Epub 2004 Dec 8.
 125. Lefèvre C, Bouadjar B, Karaduman A, Jobard F, Saker S, Ozguc M, Lathrop M, Prud'homme JF, Fischer J. Mutations in ichthyin a new gene on chromosome 5q33 in  a new form of autosomal recessive congenital ichthyosis. Hum Mol Genet. 2004 Oct  15;13(20).2473-82. Epub 2004 Aug 18.
 126. Hara-Chikuma M, Takeda J, Tarutani M, Uchida Y, Holleran WM, Endo Y, Elias PM, Inoue S. Epidermal-specific defect of GPI anchor in Pig-a null mice results in Harlequin ichthyosis-like features. J Invest Dermatol. 2004 Sep;123(3).464-9.
 127. Thacher TD, Fischer PR, Pettifor JM, Darmstadt GL. Nutritional rickets in ichthyosis and response to calcipotriene. Pediatrics. 2004 Jul;114(1).e119-23.
 128. Schmuth M, Fluhr JW, Crumrine DC, Uchida Y, Hachem JP, Behne M, Moskowitz DG, Christiano AM, Feingold KR, Elias PM. Structural and functional consequences  of loricrin mutations in human loricrin keratoderma (Vohwinkel syndrome with ichthyosis). J Invest Dermatol. 2004 Apr;122(4).909-22.
 129. Klar J, Gedde-Dahl T Jr, Larsson M, Pigg M, Carlsson B, Tentler D, Vahlquist A, Dahl N. Assignment of the locus for ichthyosis prematurity syndrome to chromosome 9q33.3-34.13. J Med Genet. 2004 Mar;41(3).208-12.
 130. Gånemo A, Sjöden PO, Johansson E, Vahlquist A, Lindberg M. Health-related quality of life among patients with ichthyosis. Eur J Dermatol. 2004 Jan-Feb;14(1).61-6.
 131. Akiyama M, Sawamura D, Nomura Y, Sugawara M, Shimizu H. Truncation of CGI-58 protein causes malformation of lamellar granules resulting in ichthyosis in Dorfman-Chanarin syndrome. J Invest Dermatol. 2003 Nov;121(5).1029-34.
 132. Naik NS. Annular epidermolytic ichthyosis. Dermatol Online J. 2003 Oct;9(4).4.
 133. Lefévre C, Audebert S, Jobard F, Bouadjar B, Lakhdar H, Boughdene-Stambouli  O, Blanchet-Bardon C, Heilig R, Foglio M, Weissenbach J, Lathrop M, Prud'homme JF, Fischer J. Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2. Hum Mol Genet. 2003 Sep 15;12(18).2369-78. Epub 2003 Jul 15.
 134. Zeeuwen PL, Dale BA, de Jongh GJ, van Vlijmen-Willems IM, Fleckman P, Kimball JR, Stephens K, Schalkwijk J. The human cystatin M/E gene (CST6). exclusion candidate gene for harlequin ichthyosis. J Invest Dermatol. 2003 Jul;121(1).65-8.
 135. Ishida-Yamamoto A, Richard G, Takahashi H, Iizuka H. In vivo studies of mutant keratin 1 in ichthyosis hystrix Curth-Macklin. J Invest Dermatol. 2003 Mar;120(3).498-500.
 136. Kon A, Takeda H, Sasaki H, Yoneda K, Nomura K, Ahvazi B, Steinert PM, Hanada K, Hashimoto I. Novel transglutaminase 1 gene mutations (R348X/Y365D) in a Japanese family with lamellar ichthyosis. J Invest Dermatol. 2003 Jan;120(1).170-2.
 137. Shultz LD, Lyons BL, Burzenski LM, Gott B, Samuels R, Schweitzer PA, Dreger  C, Herrmann H, Kalscheuer V, Olins AL, Olins DE, Sperling K, Hoffmann K. Mutations at the mouse ichthyosis locus are within the lamin B receptor gene. a single gene model for human Pelger-Huët anomaly. Hum Mol Genet. 2003 Jan 1;12(1).61-9.
 138. Chittick EJ, Olivry T, Dalldorf F, Wright J, Dale BA, Wolfe BA. Harlequin ichthyosis in two greater kudu (Tragelaphus strepsiceros). Vet Pathol. 2002 Nov;39(6).751-6.
 139. Baala L, Hadj-Rabia S, Hamel-Teillac D, Hadchouel M, Prost C, Leal SM, Jacquemin E, Sefiani A, De Prost Y, Courtois G, Munnich A, Lyonnet S, Vabres P. Homozygosity mapping of a locus for a novel syndromic ichthyosis to chromosome 3q27-q28. J Invest Dermatol. 2002 Jul;119(1).70-6.
 140. van Steensel MA, van Geel M, Nahuys M, Smitt JH, Steijlen PM. A novel connexin 26 mutation in a patient diagnosed with keratitis-ichthyosis-deafness syndrome. J Invest Dermatol. 2002 Apr;118(4).724-7.
 141. Richard G, Rouan F, Willoughby CE, Brown N, Chung P, Ryynänen M, Jabs EW, Bale SJ, DiGiovanna JJ, Uitto J, Russell L. Missense mutations in GJB2 encoding connexin-26 cause the ectodermal dysplasia keratitis-ichthyosis-deafness syndrome. Am J Hum Genet. 2002 May;70(5).1341-8. Epub 2002 Mar 22.
 142. Jimenez Vaca AL, Valdes-Flores Mdel R, Rivera-Vega MR, González-Huerta LM, Kofman-Alfaro SH, Cuevas-Covarrubias SA. Deletion pattern of the STS gene in X-linked ichthyosis in a Mexican population. Mol Med. 2001 Dec;7(12).845-9.
 143. Pilgram GS, Vissers DC, van der Meulen H, Pavel S, Lavrijsen SP, Bouwstra JA, Koerten HK. Aberrant lipid organization in stratum corneum of patients with atopic dermatitis and lamellar ichthyosis. J Invest Dermatol. 2001 Sep;117(3).710-7.
 144. Yang JM, Ahn KS, Cho MO, Yoneda K, Lee CH, Lee JH, Lee ES, Candi E, Melino G, Ahvazi B, Steinert PM. Novel mutations of the transglutaminase 1 gene in lamellar ichthyosis. J Invest Dermatol. 2001 Aug;117(2).214-8.
 145. Akiyama M, Takizawa Y, Suzuki Y, Ishiko A, Matsuo I, Shimizu H. Compound heterozygous TGM1 mutations including a novel missense mutation L204Q in a mild form of lamellar ichthyosis. J Invest Dermatol. 2001 Jun;116(6).992-5.
 146. Krebsová A, Küster W, Lestringant GG, Schulze B, Hinz B, Frossard PM, Reis A, Hennies HC. Identification, by homozygosity mapping, of a novel locus for autosomal recessive congenital ichthyosis on chromosome 17p, and evidence for further genetic heterogeneity. Am J Hum Genet. 2001 Jul;69(1).216-22. Epub 2001 Jun 7.
 147. Esposito G, Auricchio L, Rescigno G, Paparo F, Rinaldi M, Salvatore F. Transglutaminase 1 gene mutations in Italian patients with autosomal recessive lamellar ichthyosis. J Invest Dermatol. 2001 May;116(5).809-12.
 148. Sprecher E, Ishida-Yamamoto A, Becker OM, Marekov L, Miller CJ, Steinert PM, Neldner K, Richard G. Evidence for novel functions of the keratin tail emerging from a mutation causing ichthyosis hystrix. J Invest Dermatol. 2001 Apr;116(4).511-9.
 149. Valdes-Flores M, Kofman-Alfaro SH, Vaca AL, Cuevas-Covarrubias SA. Deletion  of exons 1-5 of the STS gene causing X-linked ichthyosis. J Invest Dermatol. 2001 Mar;116(3).456-8.
 150. Presland RB, Boggess D, Lewis SP, Hull C, Fleckman P, Sundberg JP. Loss of normal profilaggrin and filaggrin in flaky tail (ft/ft) mice. an animal model for the filaggrin-deficient skin disease ichthyosis vulgaris. J Invest Dermatol. 2000 Dec;115(6).1072-81.
 151. Elias PM, Fartasch M, Crumrine D, Behne M, Uchida Y, Holleran WM. Origin of  the corneocyte lipid envelope (CLE). observations in harlequin ichthyosis and cultured human keratinocytes. J Invest Dermatol. 2000 Oct;115(4).765-9.
 152. Gohlke BC, Haug K, Fukami M, Friedl W, Noeker M, Rappold GA, Haverkamp F. Interstitial deletion in Xp22.3 is associated with X linked ichthyosis, mental retardation, and epilepsy. J Med Genet. 2000 Aug;37(8).600-2.
 153. Menni S, Boccardi D, Brusasco A. Ichthyosis revealing coeliac disease. Eur J Dermatol. 2000 Jul-Aug;10(5).398-9.
 154. Oyama N, Satoh M, Iwatsuki K, Kaneko F. Novel point mutations in the steroid sulfatase gene in patients with X-linked ichthyosis. transfection analysis using  the mutated genes. J Invest Dermatol. 2000 Jun;114(6).1195-9.
 155. Virolainen E, Wessman M, Hovatta I, Niemi KM, Ignatius J, Kere J, Peltonen L, Palotie A. Assignment of a novel locus for autosomal recessive congenital ichthyosis to chromosome 19p13.1-p13.2. Am J Hum Genet. 2000 Mar;66(3).1132-7.
 156. Fischer J, Faure A, Bouadjar B, Blanchet-Bardon C, Karaduman A, Thomas I, Emre S, Cure S, Ozgüc M, Weissenbach J, Prud'homme JF. Two new loci for autosomal recessive ichthyosis on chromosomes 3p21 and 19p12-q12 and evidence for further genetic heterogeneity. Am J Hum Genet. 2000 Mar;66(3).904-13.
 157. Boente MC, Bibas-Bonet H, Coronel AM, Asial RA. Atrichia, ichthyosis, follicular hyperkeratosis, chronic candidiasis, keratitis, seizures, mental retardation and inguinal hernia. a severe manifestation of IFAP syndrome? Eur J Dermatol. 2000 Mar;10(2).98-102.
 158. Valdes-Flores M, Kofman-Alfaro SH, Vaca AL, Cuevas-Covarrubias SA. Mutation  report. a novel partial deletion of exons 2-10 of the STS gene in recessive X-linked ichthyosis. J Invest Dermatol. 2000 Mar;114(3).591-3.
 159. Takizawa Y, Akiyama M, Nagashima M, Shimizu H. A novel asparagine-->aspartic acid mutation in the rod 1A domain in keratin 2e in a Japanese family with ichthyosis bullosa of Siemens. J Invest Dermatol. 2000 Jan;114(1).193-5.
 160. Parikh DA. Lamellar ichthyosis - An update. Indian J Dermatol Venereol Leprol. 2000 Jan-Feb;66(1).32-3.
 161. Laiho E, Niemi KM, Ignatius J, Kere J, Palotie A, Saarialho-Kere U. Clinical and morphological correlations for transglutaminase 1 gene mutations in autosomal recessive congenital ichthyosis. Eur J Hum Genet. 1999 Sep;7(6).625-32.
 162. Sood A, D'Souza P, Pandhi RK. Ichthyosis vulgaris involving the scalp area affected by androgenetic alopecia. Indian J Dermatol Venereol Leprol. 1999 Jul-Aug;65(4).198.
 163. Benoit B. Three-dimensional ultrasonography of congenital ichthyosis. Ultrasound Obstet Gynecol. 1999 May;13(5).380.
 164. Peña-Penabad C, de Unamuno P, García Silva J, Ludeña MD, González Sarmiento  R, Pérez-Arellano JL. Altered expression of immunoreactive involucrin in lamellar ichthyosis. Eur J Dermatol. 1999 Apr-May;9(3).197-201.
 165. Parmentier L, Clepet C, Boughdene-Stambouli O, Lakhdar H, Blanchet-Bardon C, Dubertret L, Wunderle E, Pulcini F, Fizames C, Weissenbach J. Lamellar ichthyosis. further narrowing, physical and expression mapping of the chromosome  2 candidate locus. Eur J Hum Genet. 1999 Jan;7(1).77-87.
 166. Arin MJ, Longley MA, Epstein EH Jr, Scott G, Goldsmith LA, Rothnagel JA, Roop DR. A novel mutation in the 1A domain of keratin 2e in ichthyosis bullosa of Siemens. J Invest Dermatol. 1999 Mar;112(3).380-2.
 167. Sybert VP, Francis JS, Corden LD, Smith LT, Weaver M, Stephens K, McLean WH. Cyclic ichthyosis with epidermolytic hyperkeratosis. A phenotype conferred by mutations in the 2B domain of keratin K1. Am J Hum Genet. 1999 Mar;64(3).732-8.
 168. Pigg M, Gedde-Dahl T Jr, Cox D, Hausser I, Anton-Lamprecht I, Dahl N. Strong founder effect for a transglutaminase 1 gene mutation in lamellar ichthyosis and  congenital ichthyosiform erythroderma from Norway. Eur J Hum Genet. 1998 Nov-Dec;6(6).589-96.
 169. Adams SP. Dermacase. Ichthyosis vulgaris. Can Fam Physician. 1998 Dec;44.2645, 2652.
 170. Dilek I, Demirer T, Ustün C, Arat M, Koç H, Beksaç M, Erdi H, Anadolu R, Ozcan M, Ilhan O, Akan H. Acquired ichthyosis associated with chronic graft-versus-host disease following allogeneic peripheral blood stem cell transplantation in a patient with chronic myelogenous leukemia. Bone Marrow Transplant. 1998 Jun;21(11).1159-61.
 171. Nirunsuksiri W, Zhang SH, Fleckman P. Reduced stability and bi-allelic, coequal expression of profilaggrin mRNA in keratinocytes cultured from subjects with ichthyosis vulgaris. J Invest Dermatol. 1998 Jun;110(6).854-61.
 172. Candi E, Melino G, Lahm A, Ceci R, Rossi A, Kim IG, Ciani B, Steinert PM. Transglutaminase 1 mutations in lamellar ichthyosis. Loss of activity due to failure of activation by proteolytic processing. J Biol Chem. 1998 May 29;273(22).13693-702.
 173. Hennies HC, Küster W, Wiebe V, Krebsová A, Reis A. Genotype/phenotype correlation in autosomal recessive lamellar ichthyosis. Am J Hum Genet. 1998 May;62(5).1052-61.
 174. Bichakjian CK, Nair RP, Wu WW, Goldberg S, Elder JT. Prenatal exclusion of lamellar ichthyosis based on identification of two new mutations in the transglutaminase 1 gene. J Invest Dermatol. 1998 Feb;110(2).179-82.
 175. Jeon S, Djian P, Green H. Inability of keratinocytes lacking their specific  transglutaminase to form cross-linked envelopes. absence of envelopes as a simple diagnostic test for lamellar ichthyosis. Proc Natl Acad Sci U S A. 1998 Jan 20;95(2).687-90.
 176. Choate KA, Williams ML, Khavari PA. Abnormal transglutaminase 1 expression pattern in a subset of patients with erythrodermic autosomal recessive ichthyosis. J Invest Dermatol. 1998 Jan;110(1).8-12.
 177. Laiho E, Ignatius J, Mikkola H, Yee VC, Teller DC, Niemi KM, Saarialho-Kere  U, Kere J, Palotie A. Transglutaminase 1 mutations in autosomal recessive congenital ichthyosis. private and recurrent mutations in an isolated population. Am J Hum Genet. 1997 Sep;61(3).529-38.
 178. Alperin ES, Shapiro LJ. Characterization of point mutations in patients with X-linked ichthyosis. Effects on the structure and function of the steroid sulfatase protein. J Biol Chem. 1997 Aug 15;272(33).20756-63.
 179. Sundberg JP, Boggess D, Hogan ME, Sundberg BA, Rourk MH, Harris B, Johnson K, Dunstan RW, Davisson MT. Harlequin ichthyosis (ichq). a juvenile lethal mouse  mutation with ichthyosiform dermatitis. Am J Pathol. 1997 Jul;151(1).293-310.
 180. Freiberg RA, Choate KA, Deng H, Alperin ES, Shapiro LJ, Khavari PA. A model  of corrective gene transfer in X-linked ichthyosis. Hum Mol Genet. 1997 Jun;6(6).927-33.
 181. Montague I, Fox R, Mann R. Intra-amniotic debris identified at ultrasound scanning. a feature of congenital ichthyosis. Ultrasound Obstet Gynecol. 1997 May;9(5).350-1.
 182. Malakar S, Lahiri K, Sengupta SR. Ichthyosis linearis circumflexa. Indian J  Dermatol Venereol Leprol. 1996 Nov-Dec;62(6).379-80.
 183. Parmentier L, Lakhdar H, Blanchet-Bardon C, Marchand S, Dubertret L, Weissenbach J. Mapping of a second locus for lamellar ichthyosis to chromosome 2q33-35. Hum Mol Genet. 1996 Apr;5(4).555-9. Erratum in. Hum Mol Genet 1996 Jun;5(6).862-3.
 184. Criton S, Vincent J. Keratitis, ichthyosis and deafness (KID) syndrome. Indian J Dermatol Venereol Leprol. 1995 Sep-Oct;61(5).312-3.
 185. Nirunsuksiri W, Presland RB, Brumbaugh SG, Dale BA, Fleckman P. Decreased profilaggrin expression in ichthyosis vulgaris is a result of selectively impaired posttranscriptional control. J Biol Chem. 1995 Jan 13;270(2).871-6.
 186. Russell LJ, DiGiovanna JJ, Hashem N, Compton JG, Bale SJ. Linkage of autosomal recessive lamellar ichthyosis to chromosome 14q. Am J Hum Genet. 1994 Dec;55(6).1146-52.
 187. Sharma K, Agrawal S, Sharma RK. Ichthyosis-associated spheroid corneal degeneration in HLA-DR identical brothers. Indian J Ophthalmol. 1993 Dec;41(4).191-3.
 188. Basler E, Grompe M, Parenti G, Yates J, Ballabio A. Identification of point  mutations in the steroid sulfatase gene of three patients with X-linked ichthyosis. Am J Hum Genet. 1992 Mar;50(3).483-91.
 189. Schnur RE, Trask BJ, van den Engh G, Punnett HH, Kistenmacher M, Tomeo MA, Naids RE, Nussbaum RL. An Xp22 microdeletion associated with ocular albinism and  ichthyosis. approximation of breakpoints and estimation of deletion size by using cloned DNA probes and flow cytometry. Am J Hum Genet. 1989 Nov;45(5).706-20.
 190. Mihalko M, Lindfors KK, Grix AW, Brant WE, McGahan JP. Prenatal sonographic  diagnosis of harlequin ichthyosis. AJR Am J Roentgenol. 1989 Oct;153(4).827-8.
 191. Shackleton CH, Reid S. Diagnosis of recessive X-linked ichthyosis. quantitative HPLC/mass spectrometric analysis of plasma for cholesterol sulfate.  Clin Chem. 1989 Sep;35(9).1906-10.
 192. Clayton-Smith J, Donnai D. A new recessive syndrome of unusual facies, digital abnormalities, and ichthyosis. J Med Genet. 1989 May;26(5).339-42.
 193. Boparai MS, Dash RG, Sohi BK. Lamellar ichthyosis (collodian baby) with severe bilateral ectropion. Indian J Ophthalmol. 1988 Jul-Sep;36(3).140-1.
 194. Bonifas JM, Morley BJ, Oakey RE, Kan YW, Epstein EH Jr. Cloning of a cDNA for steroid sulfatase. frequent occurrence of gene deletions in patients with recessive X chromosome-linked ichthyosis. Proc Natl Acad Sci U S A. 1987 Dec;84(24).9248-51.
 195. Ballabio A, Parenti G, Carrozzo R, Sebastio G, Andria G, Buckle V, Fraser N, Craig I, Rocchi M, Romeo G, et al. Isolation and characterization of a steroid sulfatase cDNA clone. genomic deletions in patients with X-chromosome-linked ichthyosis. Proc Natl Acad Sci U S A. 1987 Jul;84(13).4519-23.
 196. Gillard EF, Affara NA, Yates JR, Goudie DR, Lambert J, Aitken DA, Ferguson-Smith MA. Deletion of a DNA sequence in eight of nine families with X-linked ichthyosis (steroid sulphatase deficiency). Nucleic Acids Res. 1987 May  26;15(10).3977-85.
 197. Garty BZ. High plasma urea concentration in babies with lamellar ichthyosis. Arch Dis Child. 1986 Dec;61(12).1245-6.
 198. Williams ML. Dermatology. recessive x-linked ichthyosis. West J Med. 1985 Aug;143(2).229-30.
 199. Elias PM, Williams ML, Maloney ME, Bonifas JA, Brown BE, Grayson S, Epstein  EH Jr. Stratum corneum lipids in disorders of cornification. Steroid sulfatase and cholesterol sulfate in normal desquamation and the pathogenesis of recessive  X-linked ichthyosis. J Clin Invest. 1984 Oct;74(4).1414-21.
 200. Williams ML, Elias PM. Elevated n-alkanes in congenital ichthyosiform erythroderma. Phenotypic differentiation of two types of autosomal recessive ichthyosis. J Clin Invest. 1984 Jul;74(1).296-300.
 201. Muskiet FA, Jansen G, Wolthers BG, Marinkovic-Ilsen A, van Voorst Vader PC.  Gas-chromatographic determination of cholesterol sulfate in plasma and erythrocytes, for the diagnosis of recessive X-linked ichthyosis. Clin Chem. 1983 Jul;29(7).1404-7.
 202. Dowd PM, Munro DD. Ichthyosis and osteopetrosis. J R Soc Med. 1983 May;76(5).423-6.
 203. Baraitser M, Burn J, Fixsen J. A recessively inherited windmill-vane camptodactyly/ichthyosis syndrome. J Med Genet. 1983 Apr;20(2).125-7.
 204. Williams ML, Elias PM. Stratum corneum lipids in disorders of cornification. increased cholesterol sulfate content of stratum corneum in recessive x-linked ichthyosis. J Clin Invest. 1981 Dec;68(6).1404-10.
 205. Epstein EH Jr, Leventhal ME. Steroid sulfatase of human leukocytes and epidermis and the diagnosis of recessive X-linked ichthyosis. J Clin Invest. 1981 May;67(5).1257-62.
 206. Adam A. Sex ratio in families with X-linked ichthyosis. Am J Hum Genet. 1980 Sep;32(5).763-4.
 207. Harper PS, Marks R, Dykes PJ, Young ID. Ichthyosis, hepatosplenomegaly, and  cerebellar degeneration in a sibship. J Med Genet. 1980 Jun;17(3).212-5.
 208. Jöbsis AC, De Groot WP, Tigges AJ, De Bruijn HW, Rijken Y, Meijer AE, Marinkovic-Ilsen A. X-linked ichthyosis and X-linked placental sulfatase deficiency. a disease entity. Histochemical observations. Am J Pathol. 1980 May;99(2).279-89.
 209. Gladstien K, Shapiro LJ, Spence MA. Estimating sex ratio biases in X-linked  disorders. is there an excess of males in families with X-linked ichthyosis? Am J Hum Genet. 1979 Nov;31(6).741-6.
 210. Mohandas T, Shapiro LJ, Sparkes RS, Sparkes MC. Regional assignment of the steroid sulfatase-X-linked ichthyosis locus. implications for a noninactivated region on the short arm of human X chromosome. Proc Natl Acad Sci U S A. 1979 Nov;76(11).5779-83.
 211. Kubilus J, Tarascio AJ, Baden HP. Steroid-sulfatase deficiency in sex-linked ichthyosis. Am J Hum Genet. 1979 Jan;31(1).50-3.
 212. Brooks AP, Harrington CI. Acquired ichthyosis and toxic epidermal necrolysis and mesenteric reticulum cell sarcoma and malabsorption. Br Med J. 1977 Sep 17;2(6089).739-40.
 213. Chan HL, Gwee HM. Salty sweat and ichthyosis in Addison's disease. Br Med J. 1977 Jan 8;1(6053).81-2.
 214. Green MC, Alpert BN, Mayer TC. The site of action of the ichthyosis locus (ic) in the mouse, as determined by dermal-epidermal recombinations. J Embryol Exp Morphol. 1974 Dec;32(3).715-21.
 215. Majekodunmi AE, Femi-Pearse D. Ichthyosis. early manifestation of intestinal leiomyosarcoma. Br Med J. 1974 Sep 21;3(5933).724.
 216. Delaney TJ, Marks R, Gold SC. Congenital ichthyosiform erythroderma and lamellar ichthyosis. two patients contrasted. Proc R Soc Med. 1973 Dec;66(12).1173-5.
 217. Wilkinson DS. Proceedings. Lamellar ichthyosis. progress over twenty-one years. Proc R Soc Med. 1973 Oct;66(10).985.
 218. Adamson JE, Marten RH. Ichthyosis linearis circumflexa and Netherton's syndrome with idiopathic dwarfism. Proc R Soc Med. 1973 Jul;66(7).624-5.
 219. Shah AP, Shah SS, Doshi HV. Accentuation of ichthyosis vulgaris due to associated leprosy. Postgrad Med J. 1973 Apr;49(570).282-3.
 220. Moosa A. Peripheral neuropathy and ichthyosis in Krabbe's leucodystrophy. Arch Dis Child. 1971 Feb;46(245).112-3.
 221. Filippi G, Meera Khan P. Linkage studies on X-linked ichthyosis in Sardinia. Am J Hum Genet. 1968 Nov;20(6).564-9.
 222. Jay B, Blach RK, Wells RS. Ocular manifestations of ichthyosis. Br J Ophthalmol. 1968 Mar;52(3).217-26.
 223. Grice KA, Bettley FR. Skin water loss and accidental hypothermia in psoriasis, ichthyosis, and erythroderma. Br Med J. 1967 Oct 28;4(5573).195-8.
 224. Haste AR. Acquired ichthyosis from breast cancer. Br Med J. 1967 Oct 14;4(5571).96.
 225. Merrett JD, Wells RS, Kerr CB, Barr A. Discriminant function analysis of phenotype variates in ichthyosis. Am J Hum Genet. 1967 Jul;19(4).575-85.
 226. Wells RS. Ichthyosis. Br Med J. 1966 Dec 17;2(5528).1504-6.
 227. Wells RS, Kerr CB. Clinical features of autosomal dominant and sex-linked ichthyosis in an English population. Br Med J. 1966 Apr 16;1(5493).947-50.
 228. WOODS B. Acquired ichthyosis. Hodgkin's disease. Proc R Soc Med. 1962 Nov;55.963-4.
 229. ZALESKI WA. Congenital ichthyosis, mental retardation and spasticity (Sjogren-Larsson syndrome). Can Med Assoc J. 1962 May 19;86.951-4.
 230. LYNCH HT, OZER F, MCNUTT CW, JOHNSON JE, JAMPOLSKY NA. Secondary male hypogonadism and congenital ichthyosis. association of two rare genetic diseases. Am J Hum Genet. 1960 Dec;12.440-7.
 231. Richards BW. Congenital Ichthyosis, Spastic Diplegia, and Mental Deficiency. Br Med J. 1960 Sep 3;2(5200).714.
 232. Russell B. Acquired Ichthyosis Following Parapsoriasis en Plaque. Proc R Soc Med. 1956 Mar;49(3).132-3.
 233. SAVIN LH. Corneal dystrophy associated with congenital ichthyosis and allergic manifestations in male members of a family. Br J Ophthalmol. 1956 Feb;40(2).82-9.
 234. SNEDDON IB. Acquired ichthyosis in Hodgkin's disease. Br Med J. 1955 Mar 26;1(4916).763-4.
 235. CURTH HO, MACKLIN MT. The genetic basis of various types of ichthyosis in a  family group. Am J Hum Genet. 1954 Dec;6(4).371-82.
 236. DOWLING GB. Partial congenital ichthyosis. Proc R Soc Med. 1953 Jul;46(7).545.
 237. FINLAY HV, BOUND JP. Collodion skin in the neonate due to lamellar ichthyosis. Arch Dis Child. 1952 Oct;27(135).438-41.
 238. ITO M. Genetical studies on skin diseases. V. Ichthyosis. Tohoku J Exp Med.  1950 Dec 25;53(1/2).89-92.
 239. Whittle CH, Lyell A. Ichthyosis Congenita. Proc R Soc Med. 1950 Feb;43(2).65-6.
 240. Whittle CH. Alopecia, Possibly Due to Ichthyosis. Proc R Soc Med. 1944 Sep;37(11).643-4.
 241. Wigley JE. Case for Diagnosis.? Localized Ichthyosis. Proc R Soc Med. 1939 Jul;32(9).1028.
 242. Seitz RP. Congenital Ichthyosis (Collodion Skin). Cal West Med. 1936 Jun;44(6).500-3.
 243. Ellis RW. Ichthyosis Congenita. Proc R Soc Med. 1936 May;29(7).748-9.
 244. Mullen LM. Ichthyosis. Can Med Assoc J. 1936 Apr;34(4).430.
 245. Burrows A. Ichthyosis Histrix. (Familial). Proc R Soc Med. 1933 Oct;26(12).1555-6.
 246. Burrows A. Ichthyosis with Familial Tylosis and Multiple Rodent Ulcers. Proc R Soc Med. 1932 Apr;25(6).920-2.
 247. Little EG. Acquired Ichthyosis. Proc R Soc Med. 1929 Oct;22(12).1537-8.
 248. Weber FP. Unusual Recurrent Bullous Eruption in a Boy with Slight Ichthyosis. Proc R Soc Med. 1928 Apr;21(6).1078-9.
 249. Savatard L. Ichthyosis and Cancer of the Skin, with Special Refernce to Mulespinners' Cancer. Proc R Soc Med. 1927 Aug;20(10).1589-96.
 250. Cameron HC. Case of Congenital Ichthyosis and Cyclical Vomiting. Proc R Soc  Med. 1926;19(Sect Study Dis Child).41.
 251. Hudson AC. Case of Ichthyosis of the Skin, with Ectropion. Proc R Soc Med. 1926;19(Sect Ophthalmol).11.
 252. Dore SE. Ichthyosis in a Girl aged 13. Proc R Soc Med. 1924;17(Dermatol Sect).84-5.
 253. Davis OC. Case of Ichthyosis and a Congenital Heart Lesion associated with a Small Pulse. Proc R Soc Med. 1923;16(Sect Study Dis Child).80.
 254. Semon HC. Case of Unusual Localization of Ichthyosis. Proc R Soc Med. 1923;16(Dermatol Sect).94-5.
 255. Dore SE. Ichthyosis Hystrix Linearis of Palms. Proc R Soc Med. 1918;11(Dermatol Sect).99.
 256. Stowers JH. Photographs of a Severe Case of Congenital Ichthyosis. Proc R Soc Med. 1918;11(Dermatol Sect).7-8.
 257. Bunch JL. Ichthyosis associated with Long-standing Superficial Ulceration of the Tongue. Proc R Soc Med. 1915;8(Sect Study Dis Child).64-5.
 258. Goffe EG. Two Cases of Ichthyosis in a Family of Five Children. Proc R Soc Med. 1915;8(Sect Study Dis Child).63.
 259. Goffe EG. Four Cases of Ichthyosis in a Family of Six Children. Proc R Soc Med. 1915;8(Sect Study Dis Child).63.
 260. Bunch JL. Generalized Ichthyosis. Proc R Soc Med. 1915;8(Sect Study Dis Child).27-8.
 261. Pernet G. Bullous Ichthyosis. Proc R Soc Med. 1914;7(Dermatol Sect).254-5.
 262. Morris M. Ichthyosis. Proc R Soc Med. 1912;5(Dermatol Sect).201.
 263. Morris M, Dore SE. Ichthyosis with Late Development. Proc R Soc Med. 1912;5(Dermatol Sect).154-5.
 264. Williams AW. Case of Ichthyosis. Proc R Soc Med. 1912;5(Dermatol Sect).146.
 265. Bunch JL. Generalized Ichthyosis in a Girl, aged 14. Proc R Soc Med. 1912;5(Dermatol Sect).134.
 266. Fox TC. Ichthyosis in a Child, aged 16 Months, treated by Thyroid Extract. Proc R Soc Med. 1911;4(Dermatol Sect).72-3.
 267. Adamson HG. Secondary Syphilis in which fading Roseola simulated Ichthyosis. Proc R Soc Med. 1911;4(Dermatol Sect).33-4.
 268. Macleod JM. Ichthyosis Follicularis in a Woman, aged 18. Proc R Soc Med. 1911;4(Dermatol Sect).131-2.
 269. Adamson HG. Keratosis Palmaris et Plantaris Associated with Generalized Ichthyosis. Proc R Soc Med. 1910;3(Dermatol Sect).83-4.
 270. Jamieson WA. Clinical Remarks ON ICHTHYOSIS AND ITS TREATMENT. Br Med J. 1907 Feb 16;1(2407).362-4.
 271. Don WW. The Action of Thyroid Extract on the Skin as Illustrated in Cases of Ichthyosis. Br Med J. 1897 Nov 6;2(1923).1334-5.
 272. Nobbs A. Thyroid Medication in Ichthyosis. Br Med J. 1895 Mar 30;1(1787).696-7.
 273. Clarke WF. Ichthyosis Linguae (So-Called) followed by Epithelioma. Br Med J. 1874 Mar 28;1(691).408.
 274. Fox T. So-Called Ichthyosis Linguae, and its Relation to Ichthyosis. Br Med  J. 1874 Mar 21;1(690).378-9.
 275. Morris H. Ichthyosis Linguae followed by Epithelioma Linguae. Br Med J. 1874 Mar 14;1(689).343.
 276. Morris H. Remarks on Ichthyosis Linguae followed by Epithelioma Linguae. With Notes of Three Cases. Br Med J. 1874 Feb 21;1(686).231-3.
 277. Clarke WF. Cases of (so-called) Ichthyosis Linguæ. Med Chir Trans. 1874;57.155-178.4.
 278. Ogle JW. Cases of Ichthyosis Spuria vel Sebacea. Med Chir Trans. 1863;46.217-22.
 279. Martin PJ. Case of Hereditary Ichthyosis. Med Chir Trans. 1818;9(Pt 1).52-294.3.