Abstract
The target brain binding site of levetiracetam (LEV) is synaptic vesicle glycoprotein 2A (SV2A). Up to now, only a homozygous pathogenic SV2A gene mutation was reported in human. We now report a novel heterozygous pathogenic SV2A gene mutation both in a girl and her mother result in epilepsy and poor response to LEV. Furthermore, the girl developed a new seizure type after using LEV. Our report had a clinical relevance that LEV could potentially produce contradictory efficacy in patients with SV2A gene mutation. If patients’ seizures became exacerbated while using LEV, SV2A gene testing is recommended.
| Original language | English |
|---|---|
| Pages (from-to) | 64-66 |
| Number of pages | 3 |
| Journal | Clinical Neurology and Neurosurgery |
| Volume | 181 |
| DOIs | |
| State | Published - Jun 2019 |
| Externally published | Yes |
Keywords
- Levetiracetam
- Myoclonus
- Novel mutation
- SV2A
- Spasm
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