Correlation of early neurodevelopmental features of children with SYNGAP1 variants and their genotypes.
10.3760/cma.j.cn511374-20230214-00074
- Author:
Haoran LIU
1
,
2
;
Shenghai YANG
;
Jiayi LI
;
Hua XIE
;
Xiaoli CHEN
Author Information
1. Genetics Research Unit, Capital Institute of Pediatrics, Beijing 100020, China. xiaolichen@pumc.edu.cn
2. xiehua_2005@126.com.
- Publication Type:Journal Article
- MeSH:
Child, Preschool;
Female;
Humans;
Infant;
Male;
Epilepsy/genetics*;
Genetic Testing;
Genotype;
Neurodevelopmental Disorders/genetics*;
ras GTPase-Activating Proteins/genetics*;
Seizures/genetics*
- From:
Chinese Journal of Medical Genetics
2024;41(1):25-31
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To explore the early neurodevelopmental features of young children with SYNGAP1 variants and their genotype-phenotype correlation.
METHODS:Young children with neurodevelopmental disorders (NDDs) (< 5 years old) who were referred to the Children's Hospital Affiliated to the Capital Institute of Pediatrics between January 2019 and July 2022 were selected as the study subjects. All children had undergone whole-exome sequencing, comprehensive pediatric neuropsychological assessment, familial segregation analysis, and pathogenicity classification. Meanwhile, young Chinese NDD children (< 5 years old) with pathogenic/likely pathogenic SYNGAP1 variants were retrieved from the literature, with information including detailed clinical and genetic testing, neurodevelopmental quotient (DQ) of the Children Neuropsychological and Behavior Scale-Revision 2016 (CNBS-R2016). Children who did not have a detailed DQ but had their developmental status assessed by a medical professional were also included. The correlation between neurodevelopmental severity, comorbidity and SYNGAP1 variants were summarized.
RESULTS:Four young NDD children carrying SYNGAP1 variants were recruited (1 male and 3 females, with a mean age of 34.0 ± 18.2 months), among whom one harboring a novel variant (c.437C>G, p.S146*). Combined with 19 similar cases retrieved from the literature, 23 Chinese NDD young children were included in our study (8 males and 10 females, 5 with unknown sex, with a mean age of 37.1 ± 14.2 months). A loss of function (LOF) variant was found in 19 (82.6%) children. All of the children had presented global developmental delay (GDD) before the age of two. In addition, 16 (69.6%) had seizure/epilepsy at the age of 27.0 ± 12.1 months, among whom 15 had occurred independent of the global developmental delay. Myoclonic and absence were common types of seizures. Compared with those with variants of exons 8 to 15, the severity of developmental delay was milder among children with variants in exons 1 to 5.
CONCLUSION:The early neurodevelopment features of the SYNGAP1 variants for young children (< 5 years old) have included global developmental delay and seizure/epilepsy. All of the children may present GDD before the age of two. The severity of developmental delay may be related to the type and location of the SYNGAP1 variants.
