Megacystis–microcolon–intestinal hypoperistalsis syndrome in a male infant
✍ Scribed by Deborah A. Willard; Orlando F. Gabriele
- Publisher
- John Wiley and Sons
- Year
- 1986
- Tongue
- English
- Weight
- 295 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0091-2751
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✦ Synopsis
The megacystis-microcolon-intestinal hypoperistalsis (MMIH) syndrome in five female infants was first described by Berdon et all in 1976. This syndrome has since been described in seven additional female infantsZ8 and two male infants.'~~ The prenatal ultrasound appearance was described in four of these infant^.^.^ A case of MMIH in a male infant is presented.
📜 SIMILAR VOLUMES
The megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS) is a rare congenital complex originally described in 1976 by Berdon et al.' Although 17 cases of MMIHS have been described since this original publication, few have emphasized the importance of antenatal sonographic diagnosis for