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Piebaldisme: une anomalie pigmentaire à reconnaitre: à propos d'un cas et revue de la littérature

Piebaldism is a rare autosomal dominant disorder characterized by an abnormal congenital skin pigmentation causing hypopigmented areas. It is due to an abnormal melanocytes development. It usually affects only the skin, but it may be associated with other anomalies or confused with other differentia...

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Detalles Bibliográficos
Autores principales: El Kouarty, Hajar, Dakhama, Badr Sououd Benjelloun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5326035/
https://www.ncbi.nlm.nih.gov/pubmed/28292117
http://dx.doi.org/10.11604/pamj.2016.25.155.10499

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