Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly, and facial dysmorphism

Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly, and facial dysmorphism

Objective: To present prenatal diagnosis of mosaic trisomy 2. Materials and Methods: A 29-year-old woman underwent amniocentesis at 17 weeks of gestation because of abnormal maternal serum screening, and the cytogenetic result was 47,XY,+2[8]/46,XY[22]. She underwent repeated amniocentesis at 19 wee...

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Bibliographic Details
Main Authors: Chih-Ping Chen, Yi-Yung Chen, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Yu-Ting Chen, Chen-Chi Lee, Li-Feng Chen, Wayseen Wang
Format: Article
Language:English
Published: Elsevier 2013-09-01
Series:Taiwanese Journal of Obstetrics & Gynecology
Subjects:
amniocentesis
cytogenetic discrepancy
mosaic trisomy 2
prenatal diagnosis
trisomy 2
Online Access:http://www.sciencedirect.com/science/article/pii/S1028455913001241

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http://www.sciencedirect.com/science/article/pii/S1028455913001241

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