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- W2000480163 abstract "Hemiplegic migraine (HM) is a rare migraine subtype characterized by hemiparesis during the attack and is associated with at least 3 genes: CACNA1A , ATP1A2, and SCN1A .1 Recent reports suggested that the proline-rich transmembrane protein PRRT2 gene might be the fourth gene for HM.2 In the vast majority of cases, PRRT2 is associated with paroxysmal kinesigenic dyskinesia, benign familial infantile seizures (BFIS), or infantile convulsion choreoathetosis syndrome. In families with such a “typical PRRT2 phenotype,” HM was reported in a few PRRT2 mutation carriers. Most of these cases also had a “typical PRRT2 phenotype.”2 Vice versa, PRRT2 mutations were found in 5 out of over 200 index cases with HM; 2 of these 5 PRRT2 mutation carriers also had features of “typical PRRT2 phenotypes.”3,4" @default.
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- W2000480163 date "2014-06-13" @default.
- W2000480163 modified "2023-09-23" @default.
- W2000480163 title "PRRT2 and hemiplegic migraine: A complex association" @default.
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- W2000480163 doi "https://doi.org/10.1212/wnl.0000000000000590" @default.
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