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Case of Waardenburg Shah syndrome in a family with review of literature
Waardenburg syndrome is a rare disease characterized by sensorineural deafness in association with pigmentary defects. Depending on additional symptoms, WS have been classified into four types. Waardenburg syndrome type 4, also called as Waardenburg Shah Syndrome is a very rare congenital disorder w...
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| Publicat a: | J Otol |
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| Autor principal: | |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Chinese PLA General Hospital
2018
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6291636/ https://ncbi.nlm.nih.gov/pubmed/30559775 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.joto.2018.05.005 |
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