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Megacystis-microcolon-intestinal hypoperistalsis syndrome associated with prune belly syndrome: a case report.

Abstract
Megacystis Microcolon Intestinal Hypoperistalsis Syndrome is a quite rare congenital anomaly that presents with a functional obstruction of the gastrointestinal tract which is usually fatal. It is three to four times more prevalent in females. We present a case of a rare association of a male neonate with Megacystis Microcolon Intestinal Hypoperistalsis Syndrome who in addition had the classical triad of Prune Belly Syndrome and thus suggest a possibility of different spectrums with a common pathogenesis.
AuthorsTanveer Akhtar, Anand Alladi, O S Siddappa
JournalJournal of neonatal surgery (J Neonatal Surg) Vol. 1 Issue 2 Pg. 26 ( 2012) ISSN: 2226-0439 [Print] Pakistan
PMID26023385 (Publication Type: Case Reports)

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