Analysis of KIAA0196 gene mutation in a family with hereditary spastic paraplegia.
10.3760/cma.j.issn.1003-9406.2019.06.013
- VernacularTitle:一个遗传性痉挛性截瘫家系KIAA0196基因的突变分析与追溯
- Author:
Gen LI
1
;
Ying QING
1
;
Xuhan YANG
1
;
Jingyu LOU
1
;
Xiaowen HU
1
;
Chao YANG
1
;
Juan ZHANG
1
;
Lin HE
1
;
Jianping LI
2
;
Chunling WAN
1
Author Information
1. Bio-X Institute, Shanghai Jiao Tong University, Shanghai 200030, China. Email: clwan@sjtu.edu.cn.
2. Department of Neurology, Renji Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai 200127, China. Email: li-jianping2007@163.com.
- Publication Type:Case Reports
- MeSH:
Adult;
Asian Continental Ancestry Group;
Heterozygote;
Humans;
Mutation;
Pedigree;
Phenotype;
Proteins;
genetics;
Spastic Paraplegia, Hereditary;
genetics
- From:
Chinese Journal of Medical Genetics
2019;36(6):584-587
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To identify pathogenic mutation in a Chinese family affected with hereditary spastic paraplegia (HSP) through genetic testing and a follow-up survey.
METHODS:Whole exome sequencing was performed on DNA samples of two patients and one unaffected member to screen candidate mutations. Sanger sequencing was used to validate the suspected mutations in all ten family members.
RESULTS:Four patients and three asymptomatic members (under 25 years old) carried a c.1771T>C mutation of the KIAA0196, while the other three asymptomatic members (over 40 years old) did not carry the mutation. The mutation was predicted to be "affect protein function", "probably damaging" and "disease causing" by SIFT, PolyPhen-2 and Mutation Taster, respectively. Three asymptomatic carriers were followed up and one of them developed HSP one year later, while the other two had no signs of the disease yet.
CONCLUSION:The clinical phenotype of the c.1771T>C mutation of KIAA0196 has a considerable heterogeneity and this mutation may be a common pathogenic site of KIAA0196 mutations among Chinese patients with hereditary spastic paraplegia.
