Clinical characteristics and genetic analysis of primary coenzyme Q10 deficiency caused by COQ4 gene mutation
10.3760/cma.j.issn.1000-6699.2019.12.004
- VernacularTitle: COQ4基因变异致原发性辅酶Q10缺乏症的临床特点和遗传学分析
- Author:
Lili GE
1
;
Chongfen CHEN
;
Lei LIU
;
Xuan ZHENG
;
Jinghui KONG
;
Yinsen SONG
Author Information
1. Henan Provincial Key Laboratory of Children′s Genetics and Metabolic Diseases, Children′s Hospital Affiliated to Zhengzhou University (Zhengzhou Children′s Hospital), Zhengzhou 450018, China
- Publication Type:Journal Article
- Keywords:
Primary coenzyme Q10 deficiency;
COQ4 gene;
Gene mutation
- From:
Chinese Journal of Endocrinology and Metabolism
2019;35(12):1014-1018
- CountryChina
- Language:Chinese
-
Abstract:
Objective:To explore the clinical and genetic characteristics of primary coenzyme Q10 deficiency caused by coenzyme Q4 (COQ4) variants.
Methods:Clinical data were collected, while COQ4 gene was sequenced.
Results:Here were reported a boy of 3 months old who came to our hospital presented with feeding difficulties, repeated respiratory infections, convulsions for 3 months. He was subsequently diagnosed as cerebral atrophy, and growth retardation. All exons were sequenced.c.211G>A(p.A71T, maternal), c. 436T>A(p.F146I, paternal) were detected. After treatment with coenzyme Q10, the convulsive symptoms improved significantly. Literature review revealed that totally 14 cases with primary coenzyme Q10 deficiency caused by COQ4 gene mutation were reported. The onset age varies from neonatal to 18 years old, and the clinical manifestations are heterogeneous, including cardiomyopathy, epilepsy, ataxia, cerebellar atrophy, respiratory insufficiency, and growth retardation.
Conclusion:For cases with atypical clinical manifestations of primary coenzyme Q10 deficiency, gene detection is helpful for an early diagnosis and treatment.
