Cloacal dysgenesis.

Abstract:

:Cloacal dysgenesis is a rare anomaly. Fifty cases have been reported in the literature. This condition differs from the usual imperforate anus. The diagnosis, evaluation, and therapeutic management require an understanding of the embryogenesis of the cloaca. The presence at birth of a single interlabial orifice or an abnormality sited anus is a surgical emergency. Early salvage of the kidneys and relieving intestinal obstruction are emphasized. There is a high incidence of multiple system congenital abnormalities.

journal_name

Obstet Gynecol

authors

Okonkwo JE,Crocker KM

subject

Has Abstract

pub_date

1977-07-01 00:00:00

pages

97-101

issue

1

eissn

0029-7844

issn

1873-233X

journal_volume

50

pub_type

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