Abstract
Background: Familial hemiplegic migraine (FHM) is a rare monogenic subtype of migraine with aura that includes motor auras. Prophylactic treatment of FHM often has marginal effects and involves a trial-and-error strategy based on therapeutic guidelines for non-hemiplegic migraine and on case reports in FHM. Methods: We assessed the response to prophylactic medication in an FHM family and sequenced the FHM2 ATP1A2 gene in all available relatives. Results: A novel p.Met731Val ATP1A2 mutation was identified. Attack frequency was reduced significantly with sodium valproate monotherapy (n=1) and attacks ceased completely with a combination of sodium valproate and lamotrigine (n=2). Conclusions:We report dramatic prophylactic effects of sodium valproate and lamotrigine in an FHM2 family, making these drugs worth considering in the treatment of other FHM patients. © International Headache Society 2014.
Author supplied keywords
Cite
CITATION STYLE
Pelzer, N., Stam, A. H., Carpay, J. A., Vries, B. D., Van Den Maagdenberg, A. M. J. M., Ferrari, M. D., … Terwindt, G. M. (2014). Familial hemiplegic migraine treated by sodium valproate and lamotrigine. Cephalalgia, 34(9), 708–711. https://doi.org/10.1177/0333102413520086
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.