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A rare case of seven siblings with Waardenburg syndrome: a case report
BACKGROUND: Waardenburg syndrome is a group of rare genetic conditions. It is determined by the absence of melanocytes from the eyes, hair, and skin. There are four types of Waardenburg syndrome with specific criteria to diagnosis the different types. The main clinical manifestations are facial abno...
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| Publicado no: | J Med Case Rep |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6032534/ https://ncbi.nlm.nih.gov/pubmed/29973257 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13256-018-1704-1 |
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