CADASIL caused by mutation of NOTCH3 gene c.697T>A: a report on a Chinese family
10.3760/cma.j.issn.1673-4165.2022.11.005
- VernacularTitle:NOTCH3基因c.697T>A突变所致CADASIL：一个中国家系报道
- Author:
Yuanyuan LI
1
;
Xu SUN
;
Xiaoyan LU
;
Lei ZHANG
;
Jiasi LI
Author Information
1. 海军军医大学第一附属医院神经内科，上海 200433
- Keywords:
CADASIL;
Receptor, Notch3;
Heterozygote;
Mutation
- From:
International Journal of Cerebrovascular Diseases
2022;30(11):822-825
- CountryChina
- Language:Chinese
-
Abstract:
Objective:To report the clinical features, imaging findings and gene mutation features of a Chinese family with cerebral autosomal dominant arteriopathy with subcritical infarcts and leukoencephalopathy (CADASIL).Methods:We summarized the clinical and imaging features of a CADASIL family confirmed by gene sequencing. NOTCH3 gene sequencing was conducted for the proband, and the structure of the protein encoded by the mutant gene was predicted. Results:The patients in this family mainly presented with recurrent lacunar infarction and hypertension, without headache and emotional disorders such as anxiety or depression. Head MRI of the proband showed multiple lacunar infarctions and extensive white matter degeneration. Susceptibility-weighted imaging showed multiple small intracranial hemorrhages. The analysis of NOTCH3 gene showed that the proband had c.697T>A mutation. The 3D structure prediction of the protein encoded by this mutation locus showed that this locus could lead to the conversion of cysteine to serine at the 233rd position. Conclusions:The patients of this CADASIL family have a c.697T>A mutation of NOTCH3 gene. This mutation may cause the change of amino acid in the structure of the wild type Notch3 protein, which may lead to increased formation of β-folding structures in the surrounding region, thus changing the structure and function of protein and causing disease.
