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Syndrome in question
Waardenburg syndrome is an inherited disease characterized by sensorineural hearing loss, pigmentation changes and minor facial malformations. It has four clinical variants. We report the case of a girl who, like her mother, was affected by this syndrome. The diagnosis was made after detection and t...
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| Publicado no: | An Bras Dermatol |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Sociedade Brasileira de Dermatologia
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4560554/ https://ncbi.nlm.nih.gov/pubmed/26375234 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1590/abd1806-4841.20153343 |
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