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.
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Authors | Tanveer Akhtar, Anand Alladi, O S Siddappa |
Journal | Journal of neonatal surgery
(J Neonatal Surg)
Vol. 1
Issue 2
Pg. 26
( 2012)
ISSN: 2226-0439 [Print] Pakistan |
PMID | 26023385
(Publication Type: Case Reports)
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