Prenatal diagnosis of microdeletion 16p13.11 combination with partial monosomy of 2q37.1-qter and partial trisomy of 7p15.3-pter in a fetus with bilateral ventriculomegaly, agenesis of corpus callosum, and polydactyly

Prenatal diagnosis of microdeletion 16p13.11 combination with partial monosomy of 2q37.1-qter and partial trisomy of 7p15.3-pter in a fetus with bilateral ventriculomegaly, agenesis of corpus callosum, and polydactyly

Objective: To present a prenatal diagnosis of microdeletion 16p13.11 with partial monosomy of 2q37.1-qter and partial trisomy of 7p15.3-pter in a fetus with bilateral ventriculomegaly, agenesis of corpus callosum, and polydactyly. Case Report: A 41-year-old well-being Taiwanese, nulligravida woman r...

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Bibliographic Details
Main Authors: Pi-Lin Sung, Chia-Ming Chang, Chih-Yao Chen, Peng-Hui Wang, Kuan-Chong Chao, Kuo-Chang Wen, Yung-Yung Cheng, Yueh-Chun Li, Chyi-Chyang Lin
Format: Article
Language:English
Published: Elsevier 2012-06-01
Series:Taiwanese Journal of Obstetrics & Gynecology
Subjects:
agenesis of corpus callosum
microdeletion 16p13.11
polydactyly
ventriculomegaly
Online Access:http://www.sciencedirect.com/science/article/pii/S1028455912000733

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