Familial hemiplegic migraine due to CACNA1A and PNKD mutations in epilepsy with forced normalization: A case report
This case illustrates a rare coexistence of familial HM, focal refractory epilepsy, and FN. It emphasizes the need for heightened clinical awareness of FN in similar complex neurogenetic disorders and highlights the importance of individualized pharmacological strategies.
Authors
- David J. Anschel
- Daniel San‐Juan (ORCID: https://orcid.org/0000-0001-6685-5851)
- Aleida Arritola-Uriarte (ORCID: https://orcid.org/0000-0003-0333-6661)
- Lenin V. Sandoval-Luna
- Antonio Guechi (ORCID: https://orcid.org/0009-0009-9672-1016)
Institutions
- Universidad de Guadalajara (MX)
- New York Institute of Technology (US)
- St. Charles Hospital (US)
- Instituto Nacional de Neurología y Neurocirugía (MX)
Publication Details
- Journal
- Medicine
- Published
- 2025-08-15
- DOI
- https://doi.org/10.1097/md.0000000000041844
- Citations
- 1
- Primary Topic
- Migraine and Headache Studies
- Type
- article
- Field-Weighted Citation Impact
- 1.47