Diagnosis of a child with mitochondrial myopathy and cerebellar atrophy with ataxia due to compound heterozygous variants of MSTO1 gene.
10.3760/cma.j.cn511374-20210319-00249
- Author:
Yang TIAN
1
;
Zhen SHI
;
Chi HOU
;
Wenjuan LI
;
Haixia ZHU
;
Xiaojing LI
;
Wenxiong CHEN
Author Information
1. Guangzhou Women and Children' s Medical Center, Guangzhou, Guangdong 510000, China. gzchcwx@126.com.
- Publication Type:Journal Article
- MeSH:
Ataxia/genetics*;
Atrophy/genetics*;
Cell Cycle Proteins/genetics*;
Child;
Cytoskeletal Proteins/genetics*;
Humans;
Infant;
Male;
Mitochondrial Myopathies;
Mutation;
Neurodegenerative Diseases;
Whole Exome Sequencing
- From:
Chinese Journal of Medical Genetics
2022;39(4):417-420
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To explore the genetic basis for a child with myopathy and cerebellar atrophy with ataxia.
METHODS:Clinical examinations and laboratory testing were carried out for the patient. The proband and the parents' genomic DNA was extracted from peripheral blood samples and subjected to trio whole-exome sequencing. Candidate variant was validated by Sanger sequencing.
RESULTS:The 1-year-and-8-month-old boy manifested motor developmental delay, ataxia, hypomyotonia, increased serum creatine kinase. Cranial MRI showed cerebellar atrophy with progressive aggravation. Genetic testing revealed that the patient has harbored compound heterozygous variants of the MSTO1 gene, namely c.13delG (p.Ala5ProfsTer68) and c.971C>T (p.Thr324Ile), which were respectively inherited from his mother and father. The former was unreported previously and was predicted to be likely pathogenic, whilst the latter has been reported previously and was predicted to be of uncertain significance.
CONCLUSION:The compound heterozygous c.13delG (p.Ala5ProfsTer68) and c.971C>T (p.Thr324Ile) variants probably underlay the disease in the proband. Above finding has enriched the spectrum of MSTO1 gene variants underlying mitochondrial myopathy and cerebellar atrophy with ataxia.
