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Syndrome Keratitis-Ichtyosis-Deafness (KID) chez un enfant togolais issu d'un mariage consanguin

Le syndrome KID est une affection génétique rare associant kératite, ichtyose et surdité. Nous rapportons un cas dont la surdité s'est compliquée de mutisme chez un enfant togolais issu d'un mariage consanguin.Il s'agissait d'une fillette de 9 ans admise en dermatologie pour une...

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Detalles Bibliográficos
Autores principales:	Kombaté, Koussak, Saka, Bayaki, Landoh, Dadja Essoya, Mouhari-Toure, Abass, Akakpo, Séfako, Belei, Eric, Gnassingbé, Wanguena, Djibril, Mohaman Awalou, Tchangaï-Walla, Kissem, Pitché, Palokinam
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	The African Field Epidemiology Network 2015
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4646290/ https://www.ncbi.nlm.nih.gov/pubmed/26664520 http://dx.doi.org/10.11604/pamj.2015.21.266.6857

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