Clinical and genetic analysis of a child with Cerebral creatine deficiency syndrome due to variant of SLC6A8 gene.
10.3760/cma.j.cn511374-20211025-00847
- Author:
Yunjiang ZHANG
1
;
Yifeng DING
;
Yijie LI
;
Shuizhen ZHOU
Author Information
1. Department of Neurology, the Affiliated Children's Hospital of Fudan University, Shanghai 201102, China. szzhou@shmu.edu.cn.
- Publication Type:Journal Article
- MeSH:
Humans;
Male;
Amino Acid Metabolism, Inborn Errors;
Brain;
Creatine/genetics*;
Heterozygote;
Mothers;
Nerve Tissue Proteins;
Plasma Membrane Neurotransmitter Transport Proteins/genetics*;
Infant
- From:
Chinese Journal of Medical Genetics
2023;40(11):1397-1403
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To explore the clinical features and genetic variant in a child with Cerebral creatine deficiency syndrome (CCDS).
METHODS:A child who had presented at the Affiliated Children's Hospital of Fudan University on March 5, 2021 was selected as the study subject. Whole exome sequencing (WES) was carried out for the child, and candidate variant was verified by Sanger sequencing. The level of creatine in the brain was determined by magnetic resonance spectroscopy.
RESULTS:The patient, a 1-year-and-10-month male, had presented with developmental delay and epilepsy. Both his mother and grandmother had a history of convulsions. MRS showed reduced cerebral creatine in bilateral basal ganglia and thalamus. The child was found to harbor a hemizygous splicing variant of the SLC6A8 gene, namely c.1767+1_1767+2insA, which may lead to protein truncation. The variant was not found in the public databases. Both his mother and grandmother were heterozygous carriers for the same variant.
CONCLUSION:The hemizygous c.1767+1_1767+2insA variant of the SLC6A8 gene probably underlay the CCDS in this child. Discovery of the novel variant has also expanded the mutational spectrum of the SLC6A8 gene.
