Mutation analysis for a Chinese family affected with Escobar syndrome by whole exome sequencing.
- VernacularTitle:应用全外显子测序技术对一个Escobar综合征家系进行基因突变分析
- Author:
Lin HU
1
;
Huanzheng LI
;
Zhaotang LUAN
;
Xueqin XU
;
Chong CHEN
;
Ke WU
;
Shaohua TANG
Author Information
- Publication Type:Journal Article
- MeSH: Abnormalities, Multiple; genetics; Adult; Asian Continental Ancestry Group; genetics; Base Sequence; DNA Mutational Analysis; Exome; Female; Heterozygote; Homozygote; Humans; Male; Malignant Hyperthermia; genetics; Molecular Sequence Data; Pedigree; Skin Abnormalities; genetics; Young Adult
- From: Chinese Journal of Medical Genetics 2017;34(2):209-212
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo carry out mutation analysis for a Chinese family affected with Escobar syndrome.
METHODSWhole exome sequencing (WES) was employed to detect potential mutation in the proband. Suspected mutations were validated by combining clinical data and result of Sanger sequencing.
RESULTSA homozygous missense mutation c.715C>T (p.R239C) was detected in the proband and his brother who was also affected. The parents and the daughters of the proband carried the heterozygous mutation c.715C>T, while other family members did not carry the mutation.
CONCLUSIONEscobar syndrome is a rare genetic disorder. WES is able to discover genetic mutation underlying this disorder and facilitate genetic counseling and prenatal diagnosis for the affected family.
