Analysis of CNTNAP1 gene variants in a Chinese pedigree affected with lethal congenital contracture syndrome type 7.
10.3760/cma.j.cn511374-20201021-00739
- Author:
Ying ZHANG
1
;
Shuya YANG
;
Xiaodong HUO
;
Shixiu LIAO
;
Qiaofang HOU
Author Information
1. Medical Genetics Institute, Henan Provincial People's Hospital, Zhengzhou, Henan 450003, China. houqf_2000@163.com.
- Publication Type:Journal Article
- MeSH:
Cell Adhesion Molecules, Neuronal;
China;
Contracture/genetics*;
Female;
Humans;
Infant, Newborn;
Mutation;
Pedigree;
Pregnancy;
Whole Exome Sequencing
- From:
Chinese Journal of Medical Genetics
2022;39(2):194-197
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To explore the genetic basis for a couple who had developed polyhydramnios during three pregnancies and given birth to two liveborns featuring limb contracture, dyspnea and neonatal death.
METHODS:Whole-exome sequencing (WES) was carried out on fetal tissue and peripheral blood samples from the couple. Suspected variants were verified by Sanger sequencing.
RESULTS:The fetus was found to harbor homozygous nonsense c.3718C>T (p.Arg1240Ter) variants of the CNTNAP1 gene, which were respectively inherited from its mother and father. The variant was unreported previously. According to the guidelines of the American College of Medical Genetics and Genomics, the variant was predicted to be pathogenic (PVS1+PM2+PP4).
CONCLUSION:The novel homozygous nonsense variants of the CNTNAP1 gene probably underlay the lethal congenital contracture syndrome type 7 (LCCS7) in this pedigree. Above finding has enabled genetic counseling and prenatal diagnosis for the family.
