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...

Descripción completa

Detalles Bibliográficos
Autor principal: Al Fahaad, Hamad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Case Report
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

Internet

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

Ejemplares similares