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

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

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...

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Bibliographic Details
Main Authors: Yu-Ling Kuo, Chih-Ping Chen, Liang-Kai Wang, Tsang-Ming Ko, Tung-Yao Chang, Schu-Rern Chern, Peih-Shan Wu, Yu-Ting Chen, Shu-Yuan Chang
Format: Article
Language:English
Published: Elsevier 2014-06-01
Series:Taiwanese Journal of Obstetrics & Gynecology
Subjects:
22q11.2 deletion syndrome
congenital heart defects
prenatal diagnosis
Online Access:http://www.sciencedirect.com/science/article/pii/S1028455914000837

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http://www.sciencedirect.com/science/article/pii/S1028455914000837

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