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

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 report...

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Detalles Bibliográficos
Autor principal: Al Fahaad, Hamad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3970942/
https://www.ncbi.nlm.nih.gov/pubmed/24741331
http://dx.doi.org/10.2147/IMCRJ.S58432

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