# Aminopyridine treatment for an adult patient of developmental and epileptic encephalopathy with a gain-of-function mutation in KCNA2

**Authors:** Lehong Gao, Yu Jia, Yingxue Yang, Jia Chen, Liankun Ren

PMC · DOI: 10.1016/j.gendis.2025.101798 · 2025-08-07

## Full-text entities

- **Genes:** KCNA2 (potassium voltage-gated channel subfamily A member 2) [NCBI Gene 3737] {aka DEE32, EIEE32, HBK5, HK4, HUKIV, KV1.2}
- **Diseases:** developmental and epileptic encephalopathy (MESH:C562695)
- **Chemicals:** Aminopyridine (MESH:D000631)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC13011020/full.md

---
Source: https://tomesphere.com/paper/PMC13011020