Anorectal malformation and Down's syndrome in monozygotic twins.


Autoria(s): de Buys Roessingh A.S.; Mueller C.; Wiesenauer C.; Bensoussan A.L.; Beaunoyer M.
Data(s)

2009

Resumo

Anorectal malformation (ARM) can be divided in high, intermediate, and low forms according to the level of termination of the rectum in relation to the pubococcygeal and ischiatic lines. Patients with Down's syndrome have a high incidence of gastrointestinal anomalies, such as tracheoesophageal fistula, duodenal obstruction, annular pancreas, Hirschsprung's disease, and ARM. In these children, ARM is generally low with or without a fistula. The mode of inheritance of ARM and its genetic relation with Down's syndrome is not known, even if the association (ARM-Down's syndrome) seems not to be coincidental. We describe here a very rare case of monozygotic twins born with the association of ARM and Down's syndrome.

Identificador

http://serval.unil.ch/?id=serval:BIB_86BFD8ED29A1

isbn:1531-5037[electronic]

pmid:19231514

doi:10.1016/j.jpedsurg.2008.10.116

Idioma(s)

en

Fonte

Journal of Pediatric Surgery, vol. 44, no. 2, pp. e13-6

Palavras-Chave #Abnormalities, Multiple/surgery; Anal Canal/abnormalities; Diseases in Twins/surgery; Down Syndrome/complications; Humans; Infant, Newborn; Male; Rectum/abnormalities; Rectum/surgery
Tipo

info:eu-repo/semantics/article

article