View source for Medicine:Keratitis–ichthyosis–deafness syndrome

{{Infobox medical condition (new)
| name          = Keratitis-ichthyosis-deafness syndrome
| synonyms      = "Erythrokeratodermia progressiva Burns",<ref name="Bolognia">{{cite book |author=Rapini, Ronald P. |author2=Bolognia, Jean L. |author3=Jorizzo, Joseph L. |title=Dermatology: 2-Volume Set |publisher=Mosby |location=St. Louis |year=2007 |pages=770 |isbn=978-1-4160-2999-1 }}</ref> "Ichthyosiform erythroderma, corneal involvement, and deafness"
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'''Keratitis–ichthyosis–deafness syndrome''' (KID syndrome), also known as '''ichthyosiform erythroderma, corneal involvement, and deafness''', presents at birth/infancy and is characterized by progressive corneal opacification, either mild generalized hyperkeratosis or discrete erythematous plaques, and neurosensory deafness.<ref name="Fitz2">Freedberg, et al. (2003). ''Fitzpatrick's Dermatology in General Medicine''. (6th ed.). McGraw-Hill. {{ISBN|0-07-138076-0}}.</ref>{{rp|483,513}}<ref name="Andrews">James, William; Berger, Timothy; Elston, Dirk (2005). ''Andrews' Diseases of the Skin: Clinical Dermatology''. (10th ed.). Saunders. {{ISBN|0-7216-2921-0}}.</ref>{{rp|565}}

It is caused by a mutation in [[Biology:GJB2|connexin 26]].<ref>{{cite web|title=Hystrix-like ichthyosis with deafness|url=http://ghr.nlm.nih.gov/condition/hystrix-like-ichthyosis-with-deafness|website=Genetics Home Reference|publisher=U.S. National Library of Medicine|access-date=8 August 2014}}</ref>

== See also ==
* [[Medicine:Senter syndrome|Senter syndrome]]
* [[Medicine:Ichthyosis hystrix|Ichthyosis hystrix]]
* List of cutaneous conditions

== References ==
{{reflist}}

== External links ==
{{Medical resources
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|  OMIM           = 148210
|  OMIM_mult      = {{OMIM|242150||none}} 
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{{Channelopathy}}

{{DEFAULTSORT:Keratitis-ichthyosis-deafness syndrome}}
[[Category:Genodermatoses]]
[[Category:Rare syndromes]]



{{Sourceattribution|Keratitis–ichthyosis–deafness syndrome}}