A case of Cockayne syndrome caused by ERCC8 gene mutation
10.3969/j.issn.1000-3606.2017.11.004
- VernacularTitle:Cockayne综合征1例临床及ERCC8基因突变特征
- Author:
Xiuwei MA
1
;
Jiayan ZHAO
;
Ruijie GU
;
Zhichun FENG
Author Information
1. 陆军总医院附属八一儿童医院神经发育科 北京 100700
- Keywords:
Cockayne syndrome;
clinical feature;
ERCC8 gene;
gene mutation
- From:
Journal of Clinical Pediatrics
2017;35(11):815-819
- CountryChina
- Language:Chinese
-
Abstract:
Objective To explore the clinical,radiological and gene mutation features ofERCC8 gene in one patient with Cockayne syndrome.Methods Clinical and radiological data of a girl diagnosed with Cockayne syndrome through gene detection were retrospectively analyzed.Next-generation sequencing was used to detect genetic cause.Sanger sequencing was used to confirm the candidate variants and detect mutations in her parents and sister.ResuRs The patient showed psychomotor retardation,growth failure,special face,and light sensitivity.Neurological examination revealed noticeable developmental delay,motor impairment,spastic paralysis,and cerebellar ataxia.Brain MRI revealed symmetrical demyelination of bilateral centrum semiovale and periventricular white matter.The cerebellum was atrophic.The patient was found to have compound heterozygous mutations of c.397C＞T(p.Q133X) and c.394_398del(p.L132fs).Sanger sequencing showed these two mutations were inherited from her mother and father respectively.Conclusions Next-generation sequencing technology is a useful tool for the detection of mutation in ERCC8 gene,which is valuable for the diagnosis of Cockayne syndrome.These two mutations expanded the mutation spectrum of Cockayne syndrome in Chinese population.
