A case of genetic epilepsy with febrile seizures plus caused by dual variations in GABRG2 and SCN1A and a genotype-phenotype study of the family
Objective To investigate the phenotypic impact of dual variations in GABRG2 and SCN1A on genetic epilepsy with febrile seizures plus (GEFS+). Methods The clinical data of a 3-year-old girl and her three generations of family members who visited the Pediatric Internal Medicine Department due to "repe...
Sábháilte in:
| Príomhchruthaitheoir: | |
|---|---|
| Formáid: | Artigo |
| Teanga: | Chinês |
| Foilsithe / Cruthaithe: |
Editorial Office of Journal of Clinical Pediatrics
2026-01-01
|
| Sraith: | Linchuang erke zazhi |
| Ábhair: | |
| Rochtain ar líne: | https://jcp.xinhuamed.com.cn/fileup/1000-3606/PDF/1767591125376-2108603087.pdf |
| Clibeanna: |
Níl clibeanna ann, Bí ar an gcéad duine le clib a chur leis an taifead seo!
|