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Hirschsprung's Disease and Congenital Deafness
An association of Hirschsprung's disease (congenital intestinal aganglionosis) and profound congenital deafness is described in four unrelated patients and another reported case which was found in the literature. It is suggested that this might represent a new syndrome.
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| Publicado en: | J Med Genet |
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| Autores principales: | , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
BMJ Publishing Group
1973
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1013052/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/4774830/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.10.4.337 |
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