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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...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
The African Field Epidemiology Network
2016
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| 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 |