Prenatal diagnosis of a de novo 9p terminal chromosomal deletion in a fetus with major congenital anomalies
Objective: We describe a prenatal ultrasonography diagnosis of omphalocele and symbrachydactyly in a fetus and review the literature on prenatal diagnosis of 9p terminal chromosomal deletions. Case report: A 31-year-old woman (gravida 3, para 1) was referred for genetic counseling because a fetal om...
| Main Authors: | , , , , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2014-12-01
|
| Series: | Taiwanese Journal of Obstetrics & Gynecology |
| Subjects: | |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S102845591400196X |