Analysis of DFNA5 gene variant in a Chinese pedigree affected with late-onset non-syndromic hearing loss.
10.3760/cma.j.cn511374-20200331-00224
- Author:
Nuoyang WANG
1
;
Canming CHEN
;
Ming TONG
;
Qian LI
;
Li LIU
;
Suwei HU
Author Information
1. Department of Ophthalmology and Otorhinolaryngology, Yangzhou Maternal and Child Health Care Hospital, the Affiliated Hospital of Yangzhou University Medical College, Yangzhou, Jiangsu 225002 China. husuwei2004@126.com.
- Publication Type:Journal Article
- MeSH:
Age of Onset;
China;
Hearing Loss, Sensorineural/genetics*;
Humans;
Male;
Mutation;
Pedigree;
Receptors, Estrogen/genetics*
- From:
Chinese Journal of Medical Genetics
2021;38(2):174-177
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To explore the genetic basis for a Chinese pedigree affected with autosomal dominant late-onset non-syndromic hearing loss (NSHL).
METHODS:Clinical data of the pedigree were collected. Genomic DNA was extracted from peripheral blood samples of the proband and other family members. Trio whole exome sequencing was carried out for 19 396 genes to identify potential pathogenic variants. Sanger sequencing was carried out to verify the candidate variant in the pedigree.
RESULTS:The proband and his father were found to carry a c.1183+1delG p.? variant of the DFNA5 gene. The variant was confirmed to be co-segregating with the disease phenotype in the pedigree.
CONCLUSION:The c.1183+1delG p.? variant of the DFNA5 gene probably underlay the late onset NSHL in this pedigree. Above finding has enabled accurate genetic counseling for this pedigree.
