Analysis of clinical features and genetic variants in a Chinese pedigree affected with tuberous sclerosis.
10.3760/cma.j.cn511374-20200519-00355
- Author:
Haiyan MI
1
;
Yongjun CHEN
;
Shilin QI
;
Xijin LIU
;
Min LI
;
Yang SHEN
;
Shiyang LIU
Author Information
1. Department of Nephrology, Nanhua Hospital Affiliated to South China University, Hengyang, Hunan 421002, China. chenyj-usc@foxmail.com.
- Publication Type:Journal Article
- MeSH:
China;
Humans;
Mutation;
Pedigree;
Tuberous Sclerosis/genetics*;
Tuberous Sclerosis Complex 2 Protein/genetics*
- From:
Chinese Journal of Medical Genetics
2021;38(4):363-365
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To analyze the clinical features of a Chinese pedigree affected with tuberculosis sclerosis and explore its molecular pathogenesis.
METHODS:Clinical data of the proband and members of his pedigree were collected. Whole exome sequencing was carried out to detect variants of the TSC1 and TSC2 genes. Candidate variants was verified by Sanger sequencing and bioinformatic analysis.
RESULTS:The proband and his mother, who also had mild features of tuberous sclerosis, were found to harbor a novel heterozygous c.4183C>T (p.Q1395X) variant of the TSC2 gene, which was absent in the 4 healthy relatives. Bioinformatic analysis suggested the variant to be likely pathogenic.
CONCLUSION:The heterozygous c.4183C>T (p.Q1395X) variant of the TSC2 gene probably underlay the disease in this pedigree. Above finding has expanded the spectrum of TSC2 gene variants. The more severe symptoms in the proband may be attributed to phenotypic heterogeneity of this disease.
