Analysis of clinical characteristics and genetic variants in two children with Limb-girdle muscular dystrophy autosomal recessive 9 FKRP-related.
10.3760/cma.j.cn511374-20220929-00657
- Author:
Jie YU
1
;
Min XU
;
Le DING
;
Yanjun HUANG
;
Hu GUO
;
Yan HE
Author Information
1. Department of Neurology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu 210008, China. 191798047@qq.com.
- Publication Type:Journal Article
- MeSH:
Humans;
Child;
Asian People/genetics*;
Genetic Testing;
Muscular Dystrophies, Limb-Girdle/genetics*;
Muscular Dystrophy, Duchenne;
Pentosyltransferases/genetics*
- From:
Chinese Journal of Medical Genetics
2023;40(10):1217-1221
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To explore the correlation between clinical manifestations of Limb-girdle muscular dystrophy autosomal recessive 9 FKRP-related (R9 FKRP-related) and variants of the FKRP gene.
METHODS:Two children who had presented at the Children's Hospital of Nanjing Medical University respectively due to increased serum myocardial zymogram and hepatic dysfunction on September 30, 2018 and August 3, 2018 were selected as the study subjects. Clinical data of the children were collected. Both children were suspected for Duchenne or Becker muscular dystrophy for asymptomatic high creatine kinase (CK) levels. Peripheral blood samples of the children and their parents were collected for whole exome sequencing, and candidate variants were validated by Sanger sequencing.
RESULTS:Genetic testing revealed that both children have carried compound heterozygous variants of the FKRP gene. The c.545A>G and c.941C>T variants in child 1 have been reported previously, among which the c.545A>G is a hot spot mutation in the Chinese population. Child 2 has carried c.602T>C and c.961G>A variants, both of which were unreported previously.
CONCLUSION:Both children have met the diagnostic criteria for LGMD R9 FKRP-related. Carriers of the c.545A>G variant may present milder symptoms. Compared with patients carrying null variants, carriers of compound heterozygous missense variants may present with a milder phenotype, manifesting as asymptomatic high CK level.
