PRRT2 and migraine disorder: The strong genetic evidence about migraine disorders regards hemiplegic migraine, which is a rare monogenic subtype characterized by migraine with aura associated with hemiparesis mainly due to mutations in three genes—CACNA1A, ATP1A2 and SCN1A (other pathogenic variants are found in PRRT2, PNKD, SLC2A1, SLC1A3, SLC4A4 genes) [98].