Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 3 of 3 for KID "keratitis," "ichthyosis," deafness syndrome OR ichthyosis
  1. Keratitis-ichthyosis-deafness syndrome 
    Keratitis-ichthyosis-deafness (KID) syndrome is characterized by eye problems, skin abnormalities, and hearing loss.People with KID syndrome usually ... gene mutations. Ichthyosiform erythroderma, corneal involvement, and ... Genetic Testing Registry: Autosomal recessive keratitis-ichthyosis- ...
    https://medlineplus.gov/.../keratitis-ichthyosis-deafness-syndrome - Genetics
  2. GJB2 gene 
    ... HID.Because the D50N mutation can also cause keratitis-ichthyosis-deafness (KID) syndrome (described below), many researchers categorize KID syndrome ... gene mutations have been identified in people with keratitis-ichthyosis-deafness (KID) syndrome, with the most common being the D50N ...
    https://medlineplus.gov/genetics/gene/gjb2 - Genetics
  3. Hystrix-like ichthyosis with deafness 
    ... identified in people with HID also occurs in keratitis-ichthyosis-deafness syndrome (KID syndrome), a disorder with similar features and the ...
    https://medlineplus.gov/.../hystrix-like-ichthyosis-with-deafness - Genetics