Identification of two novel Parkin gene mutations in a patient affected with Juvenile Parkinson's syndrome.
10.3760/cma.j.issn.1003-9406.2019.04.013
- Author:
Li WANG
1
;
Guiyu LOU
;
Shasha BIAN
;
Litao QIN
;
Ke YANG
;
Bing ZHANG
;
Shixiu LIAO
Author Information
1. Institute of Medical Genetics of Henan Province, People's Hospital of Zhengzhou Unistersity, Henan Provincial People's Hospital, Zhengzhou, Henan 450003, China. Email: ychslshx@126.com.
- Publication Type:Case Reports
- MeSH:
Adolescent;
Base Sequence;
Female;
Humans;
Mutation;
Parkinson Disease;
Ubiquitin-Protein Ligases;
Whole Exome Sequencing
- From:
Chinese Journal of Medical Genetics
2019;36(4):344-347
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To explore the clinical and genetic features of a patient suspected with Juvenile Parkinson's syndrome (JP).
METHODS:Clinical features of the patient were analyzed. Genomic DNA of the patient and his parents was extracted from peripheral blood samples and sequenced by exome capture sequencing. The nature and impact of detected mutations were predicted and validated.
RESULTS:The patient displayed typical features including resting tremor, bradykinesia, rigidity, but with excellent response to low dose levodopa. DNA sequencing showed that she has carried compound heterozygous mutations of the Parkin gene, namely c.1381dupC and c.619-1G>C, which were respectively inherited from his mother and father. Neither mutation was reported previously. Bioinformatic analysis predicted that both mutations are pathogenic.
CONCLUSION:The patient has JP caused by mutations of the Parkin gene. Exome capture sequencing is an accurate and efficient method for genetic diagnosis of such disease.
