Genetic analysis of a pedigree affected with distal hereditary motor neuronopathy V.
10.3760/cma.j.issn.1003-9406.2019.03.004
- Author:
Tao LI
1
;
Xue LYU
;
Hai XIAO
;
Liuyi LI
;
Qiannan GUO
;
Hongdan WANG
;
Bo ZHANG
;
Chaoyang ZHANG
;
Xin WANG
;
Shixiu LIAO
Author Information
1. Department of Laboratory Medicine, Fuwai Central China Cardivascular Hospital (The Heart Center of Henan Provincial People's Hospital), Zhengzhou, Henan 451478, China. hnsyylt@126.com.
- Publication Type:Journal Article
- MeSH:
Female;
GTP-Binding Protein gamma Subunits;
Humans;
Muscular Atrophy, Spinal;
Mutation;
Pedigree;
Pregnancy
- From:
Chinese Journal of Medical Genetics
2019;36(3):207-211
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To carry out genetic testing for a family affected with distal hereditary motor neuronopathy V (dHMN V).
METHODS:Potential mutations of the GARS and BSCL2 genes were analyzed with PCR and Sanger sequencing. Suspected mutation was verified among unaffected members of the family and 100 healthy controls. Prenatal diagnosis was provided based on the above results.
RESULTS:Sequencing analysis has identified a heterozygous c.269C>T (p.S90L) mutation in the BSCL2 gene, which resulted in replacement of Serine (TCG) to Leucine (TTG). The same mutation was found in all other 3 patients from the pedigree but not among unaffected members or the 100 healthy controls. By prenatal diagnosis, the fetus did not carry the above mutation.
CONCLUSION:Pathogenic mutation of BSCL2 gene probably underlies the dHMN V in this pedigree, which enabled prenatal diagnosis for the proband.
