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Keratitis-ichthyosis-deafness syndrome
Other names	Erythrokeratodermia progressiva Burns, ichthyosiform erythroderma, corneal involvement, and deafness, KID syndrome.
This condition is inherited in an autosomal dominant manner.
Specialty	Medical genetics

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. It is caused by a mutation in connexin 26.

See also

• Senter syndrome
• Ichthyosis hystrix
• List of cutaneous conditions

References

1. Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. p. 770. ISBN 978-1-4160-2999-1.
2. Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. ISBN 0-07-138076-0.
3. James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. ISBN 0-7216-2921-0.
4. "Hystrix-like ichthyosis with deafness". Genetics Home Reference. U.S. National Library of Medicine. Retrieved 8 August 2014.

External links

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• Palmoplantar keratodermas
• Genodermatoses
• Rare syndromes
• Genodermatoses stubs