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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...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2018
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6032534/ https://www.ncbi.nlm.nih.gov/pubmed/29973257 http://dx.doi.org/10.1186/s13256-018-1704-1 |