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Piebaldisme: une génodermatose rare
Piebaldism is a rare autosomal dominant genodermatosis. It is due to congenital absence of melanocytes in the affected areas. We report a case. A 5 year old girl born to consanguineous parents and with similar cases in her mother’s; she presented since birth achromic lesions on the legs with a stead...
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| Pubblicato in: | Pan Afr Med J |
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| Autori principali: | , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
The African Field Epidemiology Network
2017
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5622833/ https://ncbi.nlm.nih.gov/pubmed/28979623 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.11604/pamj.2017.27.221.4961 |
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