suggestive of a gastro-intestinal lesion containing echogenic debris. Amniocentesis showed a normal karyotype, no cystic fibrosis mutations (70 analysed) and an AFP of 5.02 MOM. Acetylcholinesterase was weakly positive. 11 days later an intra-uterine demise was diagnosed. A 355 g fetus was delivered
Familial abdominal wall defects
β Scribed by Hershey, Douglas W. ;Haesslein, Hanns C. ;Marr, Clifford C. ;Adkins, John C.
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- English
- Weight
- 350 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0148-7299
No coin nor oath required. For personal study only.
β¦ Synopsis
We report 2 families, each having multiple sibs with abdominal wall defects. In family 1, normal parents gave birth to identical (monochorionic, diamniotic) twins. This is the first reported case of gastroschisis occurring in monozygotic twins. In family 2, a normal mother gave birth to a son with omphalocele.
Two subsequent pregnancies with a different husband resulted in a stillborn girl with partial atresia of the colon and a liveborn girl with gastroschisis. In neither case were there any associated anomalies. In neither of the 2 families was there consanguinity or history of other abdominal wall defects. The familial occurrence of these defects suggests that 1) multifactorial determination should be considered in at least some cases of abdominal wall defects, 2) the bowel atresias that occasionally accompany gastroschisis may also have a genetic (multifactorial) cause, and 3) some cases of gastroschisis and omphalocele may have the same genetic cause.
π SIMILAR VOLUMES
The various types of abdominal wall defects are considered to differ in their etiologies, a hypothesis suggested by differences in their epidemiologies. This study examined the impact of selected demographic factors on abdominal wall defects (omphalocele, gastroschisis, and body stalk anomaly) inclu