Abstract
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.
| Original language | English |
|---|---|
| Pages (from-to) | 92-96 |
| Number of pages | 5 |
| Journal | Chang Gung Medical Journal |
| Volume | 21 |
| Issue number | 1 |
| State | Published - 03 1998 |
| Externally published | Yes |