Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS): a case report.

[megacystis-microcolon-intestinal hypoperistalsis syndrome]

Megacystis-microcolon -intestinal hypoperistalsis syndrome (MMIHS ) is a rare congenital disorder characterized by a massively enlarged urinary bladder without mechanical outlet obstruction and microcolon , as well as a hypoperistaltic bowel with normal ganglion cell distribution . We report one such case to discuss the findings of antenatal ultrasound and the radiologic and pathologic features of this condition .

Diseases
Validation

Diseases presenting "congenital disorder" symptom

22q11.2 deletion syndrome

coats disease

congenital adrenal hyperplasia

cystinuria

dentinogenesis imperfecta

holt-oram syndrome

kabuki syndrome

kindler syndrome

lamellar ichthyosis

megacystis-microcolon-intestinal hypoperistalsis syndrome

oligodontia

pendred syndrome

proteus syndrome

wolf-hirschhorn syndrome

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