A Chromosomal Inversion of 46XX, inv (6) (p21.3p23) Connects to Congenital Heart Defects

A Chromosomal Inversion of 46XX, inv (6) (p21.3p23) Connects to Congenital Heart Defects

Congenital heart defects (CHDs) represent the most common human birth defects. Ventricular septal defect (VSD) is the most common subtype of CHDs. It has been shown that about 20–40% of VSDs are closely related to chromosomal aneuploidies or Mendelian diseases. In this study, we report a pedigree wi...

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Bibliographic Details
Main Authors: Liangping Cheng, Yanlai Tang, Yuese Lin, Hongjun Ba, Yiqian Ding, Dubo Chen, Min Liu, Peizhen Pan, Youzhen Qin, Zhan-Peng Huang
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-07-01
Series:Frontiers in Cardiovascular Medicine
Subjects:
congenital heart disease
ventricular septal defect
chromosomal rearrangement
human chromosome 6
proband
Online Access:https://www.frontiersin.org/article/10.3389/fcvm.2020.00121/full

Internet

https://www.frontiersin.org/article/10.3389/fcvm.2020.00121/full

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