Clinical and genetic analyses of a family with atypical nonketotic hyperglycinemia caused by compound heterozygous mutations in the GLDC gene.
- Author:
Tie-Jia JIANG
1
;
Jing-Jing JIANG
;
Jia-Lu XU
;
Jing ZHEN
;
Pei-Fang JIANG
;
Feng GAO
Author Information
1. Department of Neurology, Children's Hospital of Zhejiang University School of Medicine, Hangzhou 310051, China. epilepsy@zju.edu.cn.
- Publication Type:Case Reports
- MeSH:
Child;
Child, Preschool;
Female;
Glycine Dehydrogenase (Decarboxylating);
genetics;
High-Throughput Nucleotide Sequencing;
Humans;
Hyperglycinemia, Nonketotic;
genetics;
Male;
Mutation
- From:
Chinese Journal of Contemporary Pediatrics
2017;19(10):1087-1091
- CountryChina
- Language:Chinese
-
Abstract:
Nonketotic hyperglycinemia (NKH) is an autosomal recessive hereditary disease caused by a defect in the glycine cleavage system and is classified into typical and atypical NKH. Atypical NKH has complex manifestations and is difficult to diagnose in clinical practice. This article reports a family of NKH. The parents had normal phenotypes, and the older brother and the younger sister developed this disease in the neonatal period. The older brother manifested as intractable epilepsy, severe spastic diplegia, intellectual disability, an increased level of glycine in blood and cerebrospinal fluid, an increased glycine/creatinine ratio in urine, and an increased ratio of glycine concentration in cerebrospinal fluid and blood. The younger sister manifested as delayed language development, ataxia, chorea, mental and behavior disorders induced by pyrexia, hypotonia, an increased level of glycine in cerebrospinal fluid, and an increased ratio of glycine concentration in cerebrospinal fluid and blood. High-throughput sequencing found a maternal missense mutation, c.3006C>G (p.C1002W), and a paternal nonsense mutation, c.1256C>G (p.S419X), in the GLDC gene in both patients. These two mutations were thought to be pathogenic mutations by a biological software. H293T cells transfected with these two mutants of the GLDC gene had a down-regulated activity of glycine decarboxylase. NKH has various phenotypes, and high-throughput sequencing helps to make a confirmed diagnosis. Atypical NKH is associated with the downregulated activity of glycine decarboxylase caused by gene mutations.
