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

• Main Authors: Chih-Ping Chen (Author), Yi-Yung Chen (Author), Schu-Rern Chern (Author), Peih-Shan Wu (Author), Jun-Wei Su (Author), Yu-Ting Chen (Author), Chen-Chi Lee (Author), Li-Feng Chen (Author), Wayseen Wang (Author)
• Format: Book
• Published: Elsevier, 2013-09-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

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...