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

• المؤلفون الرئيسيون: Chih-Ping Chen (مؤلف), Yi-Yung Chen (مؤلف), Schu-Rern Chern (مؤلف), Peih-Shan Wu (مؤلف), Jun-Wei Su (مؤلف), Yu-Ting Chen (مؤلف), Chen-Chi Lee (مؤلف), Li-Feng Chen (مؤلف), Wayseen Wang (مؤلف)
• التنسيق: كتاب
• منشور في: Elsevier, 2013-09-01T00:00:00Z.
• الموضوعات: article
• الوصول للمادة أونلاين: 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...