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Megacystis-microcolon-intestinal hypoperistalsis syndrome: report of one case
Ni-Chung Lee1, Chui-Mei Tiu, Wen-Jue Soong
1Division of Pediatrics, Taipei Veterans General Hospital, No. 201 Shi-Pai Road, Sec. 2, Taipei, Taiwan.
Abstract:
Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS) is a very rare congenital disease characterized by abdominal distension due to a dilated urinary bladder, microcolon and decreased or absent intestinal peristalsis. Most patients die at an early age. We report on a female baby with this syndrome which was associated with duodenal web and tracheobronchial malacia. The literature on this syndrome is also reviewed.
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