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Waardenburg syndrome: A rare case
Waardenburg Syndrome is a rare disorder of neural crest cell development. It is genetically inherited. Varying in prevalence from 1:42000 to 1:50,000, it compromises approximately 2-5% of congenital deaf children. The syndrome is not expressed in its complete form, in about 20% cases, which adds for...
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| Publicado no: | Oman J Ophthalmol |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications & Media Pvt Ltd
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5991067/ https://ncbi.nlm.nih.gov/pubmed/29930451 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/ojo.OJO_51_2014 |
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