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1. Keratitis–ichthyosis–deafness syndrome: first affected family reported in the Middle East

Author

Al Fahaad H

Subjects
medicine.medical_specialty, Palmoplantar hyperkeratosis, Blindness, business.industry, Ichthyosis, Keratitis–ichthyosis–deafness syndrome, education, General Medicine, medicine.disease, Dermatology, humanities, Surgery, Ichthyosiform scaling, otorhinolaryngologic diseases, medicine, sense organs, business, geographic locations, Kid syndrome
Abstract

Introduction Keratitis–ichthyosis–deafness (KID) syndrome is a rare congenital multisystem disorder affecting certain tissues of ectodermal origin such as epidermis, cochlea, and cornea, leading mainly to palmoplantar hyperkeratosis, ichthyosiform scaling, deafness, and blindness. The author reports for the first time in the Middle East three family members suffering from KID syndrome in the southwestern part of Saudi Arabia.

Published
2014
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