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Rapid Communication | Open Access

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

Lehong Gaoa,b,e( ), Yu Jiaa,b,e, Yingxue Yanga,b, Jia Chena,b, Liankun Rena,b,c,d( )
Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing 100053, China
Clinical Research Center of Epilepsy, Xuanwu Hospital, Capital Medical University, Beijing 100053, China
National Center for Neurological Disorders, Beijing 100053, China
Chinese Institute for Brain Research, Beijing 102206, China

e These authors contributed equally to this work.

Peer review under the responsibility of Chongqing Medical University.

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Genes & Diseases
Volume 13 Issue 4,
July 2026
DOI: 10.1016/j.gendis.2025.101798

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Cite this article:
Gao L, Jia Y, Yang Y, et al. Aminopyridine treatment for an adult patient of developmental and epileptic encephalopathy with a gain-of-function mutation in KCNA2. Genes & Diseases, 2026, 13(4). https://doi.org/10.1016/j.gendis.2025.101798

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Received: 03 April 2025
Published: 07 August 2025
© 2026

This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).