Keratitis–Ichthyosis–Deafness: A rare kid in clinical practice

Author:

Vyas HarshitaRavindra,Shah ShikhaR,Karia UmeshK,Shah BelaJ

Publisher

Medknow

Subject

Psychiatry and Mental health,Neuropsychology and Physiological Psychology

Reference5 articles.

1. Keratitis, ichthyosis, and deafness (KID syndrome): Review of the literature and proposal of a new terminology;Caceres-Rios;Pediatr Dermatol,1996

2. Missense mutations in GJB2 encoding connexin-26 cause the ectodermal dysplasia keratitis-ichthyosis-deafness syndrome;Richard;Am J Hum Genet,2002

3. KID syndrome: A rare genodermatosis;Dey;Indian Dermatol Online J,2020

4. The keratitis, ichthyosis, and deafness (KID) syndrome;Skinner;Arch Dermatol,1981

5. Keratitis-Ichthyosis-Deafness syndrome: A rare congenital disorder;Shanker;Indian Dermatol Online J,2012

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