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Hirschsprung’s disease associated with alopecia universalis congenita: a case report
BACKGROUND: Hirschsprung’s disease is one of the commonest causes of intestinal obstruction in neonates because of gut motility disorder. It is characterized as a complex genetic heterogenous disorder with variable inheritance. Hirschsprung’s disease occurs as an isolated phenotype in majority (70 %...
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| Publicado no: | J Med Case Rep |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5025624/ https://ncbi.nlm.nih.gov/pubmed/27633379 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13256-016-1035-z |
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