Genetics and clinical phenotypes of epilepsy associated with chromosome 2q24.3 microdeletion.
10.3760/cma.j.cn112140-20220609-00527
- Author:
Na ZHAO
1
;
Miao Miao CHENG
1
;
Ying YANG
1
;
Xue Yang NIU
1
;
Yi CHEN
1
;
Xiao Ling YANG
1
;
Yue Hua ZHANG
1
Author Information
1. Department of Pediatrics, Peking University First Hospital, Bejing 100034, China.
- Publication Type:Journal Article
- MeSH:
Humans;
Abnormalities, Multiple;
Chromosomes;
DNA Copy Number Variations;
Epilepsies, Myoclonic;
Epilepsy;
Fever;
NAV1.7 Voltage-Gated Sodium Channel;
Phenotype;
Retrospective Studies;
Seizures;
Status Epilepticus;
Chromosomes, Human, Pair 2
- From:
Chinese Journal of Pediatrics
2022;60(11):1140-1146
- CountryChina
- Language:Chinese
-
Abstract:
Objective: To summarize the genetics and clinical phenotypes of epilepsy children with 2q24.3 microdeletion. Methods: All the patients with 2q24.3 microdeletion were retrospectively collected at the Pediatric Department of Peking University First Hospital from March 2017 to July 2022. The features of clinical manifestations, electroencephalogram (EEG), and neuroimaging were analyzed. Results: There were 13 patients with 2q24.3 microdeletion were included. All 13 patients had de novo copy number variation (CNV) with a deletion size ranged 0.18-7.31 Mb. The main pathogenic genes in the region were SCN3A, SCN2A, TTC21B, SCN1A and SCN9A genes. Among the 13 patients, 7 were boys, and 6 were girls. The onset age of epilepsy was 3.3(2.5, 6.0) months. Multiple seizure types were observed, including focal seizures in 13 patients, generalized tonic-clonic seizures (GTCS) in 6 patients, myoclonic seizures in 3 patients, epileptic spasm in 2 patients, and tonic seizures in 2 patients. Seizures were fever sensitivity in 9 patients. Status epilepticus was observed in 6 patients. One case had normal mental motor development and 12 cases had different degrees of developmental delay. Six patients had craniofacial abnormality, 1 had six-finger deformity of the right thumb, and 1 had multiple system abnormalities. EEG showed focal discharge in 3 cases, multifocal discharges in 5 cases, multifocal and generalized discharges in 1 case. Brain magnetic resonance imaging (MRI) showed enlargement of subarachnoid spaces in the frontal and temporal region in 4 patients, enlargement of lateral ventricle in 4 patients and delayed myelination of white matter in 1 patient. Dravet syndrome was diagnosed in 5 cases. The age at the last follow-up were 2.5(1.4,5.5) years, 1 patient was seizure free longer than 1 year, and 12 patients still had seizures. Conclusions: The epilepsy associated with 2q24.3 microdeletion is mainly induced by the deletion of SCN3A, SCN2A and SCN1A genes. The seizure onset age of 2q24.3 microdeletion related epilepsy was in infancy. Multiple seizure types are observed and the common seizure types include focal seizures and GTCS. Most patients have fever sensitivity and status epilepticus. Most patients have developmental delay. The phenotype of patients with deletion of SCN3A and SCN2A gene is more severe than that of patients with deletion of SCN1A gene only.
