Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects

• Main Authors: Yu-Ling Kuo (Author), Chih-Ping Chen (Author), Liang-Kai Wang (Author), Tsang-Ming Ko (Author), Tung-Yao Chang (Author), Schu-Rern Chern (Author), Peih-Shan Wu (Author), Yu-Ting Chen (Author), Shu-Yuan Chang (Author)
• Format: Book
• Published: Elsevier, 2014-06-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Objective: To report prenatal diagnosis of 22q11.2 deletion syndrome in a pregnancy with congenital heart defects in the fetus. Case report: A 26-year-old, primigravid woman was referred for counseling at 24 weeks of gestation because of abnormal ultrasound findings of fetal congenital heart defects...