Identification of a novel SLC26A4 mutation in a child with enlarge vestibular aqueduct syndrome.
- Author:
Donglan SUN
1
;
Weihong MU
;
Yanhua ZHANG
;
Hong GAO
;
Fang FANG
;
Mei YU
;
Lijuan ZHAO
;
Jing ZHANG
;
Dongqing MI
;
Lijia CHANG
;
Qinying CAO
Author Information
- Publication Type:Journal Article
- MeSH: Adult; Amino Acid Sequence; Child; Exons; Female; Hearing Loss, Sensorineural; genetics; Humans; Male; Membrane Transport Proteins; genetics; Molecular Sequence Data; Pedigree; Vestibular Aqueduct; abnormalities
- From: Chinese Journal of Medical Genetics 2017;34(3):390-392
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo analyze mutations of SLC26A4 gene and explore their origins for a patient with enlarge vestibuar aqueduct syndrome.
METHODSClinical data and peripheral venous blood samples were collected from the patient and her parents. Genome DNA was extracted from the peripheral blood. All of the 21 exons of the SLC26A4 gene were amplified with PCR and subjected to directly sequencing.
RESULTSThe patient was found to have carried two mutant alleles of the SLC26A4 gene, namely c.1522A to G and c.1229C to T, which were inherited from her father and mother, respectively.
CONCLUSIONSLC26A4 c.1522A to G is likely to be a pathogenic mutation. Above results may facilitate genetic counseling and prenatal diagnosis for this family.
