Analysis of genetic variant in a patient with juvenile meterochromic leukodystrophy.
10.3760/cma.j.cn511374-20211015-00818
- Author:
Xiao ZHANG
1
;
Miaomiao LI
;
Jianhua MA
;
Yucui ZANG
;
Jingli WANG
;
Yinglei XU
;
Lu SHEN
;
Shiguo LIU
Author Information
1. Department of Medical Genetics, the Affiliated Hospital of Qingdao University, Qingdao, Shandong 266000, China. liushiguo2002@126.com.
- Publication Type:Journal Article
- MeSH:
Cerebroside-Sulfatase/genetics*;
DNA;
Genetic Association Studies;
Humans;
Leukodystrophy, Metachromatic/genetics*;
Mutation
- From:
Chinese Journal of Medical Genetics
2022;39(10):1093-1098
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To explore the genetic basis for a child with metachromatic leukodystrophy (MLD).
METHODS:Clinical data of the patient was collected. Genomic DNA was extracted from peripheral blood samples of the child and his family members. Potential variant was screened by whole exome sequencing (WES), and candidate variant was verified by Sanger sequencing. The pathogenicity the variant was analyzed by multiple sequence alignment of the amino acid sequence and three-dimensional model prediction of its protein product.
RESULTS:The child was found to harbor compound heterozygous variants c.257G>A (p.R86Q) and c.467del (p.G156Afs*6) of the ARSA gene, among which the c.467del (p.G156Afs*6) frameshift variation was unreported previously. Multiple sequence alignment showed that the site of the c.257G>A (p.R86Q) missense variant is highly conserved. Three-dimensional structure modeling analysis showed that the partial deletion due to the p.G156Afs*6 variant may cause significant alteration of the structure of ARSA protein.
CONCLUSION:The discovery of novel variant in ARSA has enriched the mutational spectrum of MLD and may facilitate the understanding of the genotype-phenotype correlation of MLD.
