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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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Detalles Bibliográficos
Autores principales:	Malik, Sushma, Singhal, Mani, Jadhav, Shruti Sudhir, Korday, Charusheela Sujit, Nayak, Chitra Shivanand
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2016
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5025624/ https://www.ncbi.nlm.nih.gov/pubmed/27633379 http://dx.doi.org/10.1186/s13256-016-1035-z

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