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 %...

Descripción completa

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

Internet

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

Ejemplares similares