Megacystis-microcolon-intestinal hypoperistalsis syndrome: report of one case.

[megacystis-microcolon-intestinal hypoperistalsis syndrome]

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 .

Diseases
Validation

Diseases presenting "early age" symptom

achondroplasia

aniridia

classical phenylketonuria

cohen syndrome

congenital adrenal hyperplasia

cowden syndrome

dentin dysplasia

junctional epidermolysis bullosa

kabuki syndrome

megacystis-microcolon-intestinal hypoperistalsis syndrome

papillon-lefèvre syndrome

primary hyperoxaluria type 1

severe combined immunodeficiency

werner syndrome

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