Medicine:Keratitis–ichthyosis–deafness syndrome
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(Redirected from Medicine:Ichthyosiform erythroderma, corneal involvement, and deafness)
| Keratitis-ichthyosis-deafness syndrome | |
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| Other names | "Erythrokeratodermia progressiva Burns",[1] "Ichthyosiform erythroderma, corneal involvement, and deafness" |
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.[2]:483,513[3]:565
It is caused by a mutation in connexin 26.[4]
See also
- Senter syndrome
- Ichthyosis hystrix
- List of cutaneous conditions
References
- ↑ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. pp. 770. ISBN 978-1-4160-2999-1.
- ↑ Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. ISBN:0-07-138076-0.
- ↑ James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. ISBN:0-7216-2921-0.
- ↑ "Hystrix-like ichthyosis with deafness". U.S. National Library of Medicine. http://ghr.nlm.nih.gov/condition/hystrix-like-ichthyosis-with-deafness.
External links
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