Portal de Periódicos da CAPES

Two novel SCN1A mutations identified in families with familial hemiplegic migraine

2014; SAGE Publishing; Volume: 34; Issue: 13 Linguagem: Inglês

10.1177/0333102414529195

1468-2982

Claudia M Weller, Nadine Pelzer, Boukje de Vries, Mercè Artigas López, Oriol de Fábregues, Julio Pascual, María Antonia Ramos Arroyo, Stephany C Koelewijn, Anine H Stam, Joost Haan, Michel D. Ferrari, Gisela M. Terwindt, Arn M. J. M. van den Maagdenberg,

Vestibular and auditory disorders

Background Familial hemiplegic migraine (FHM) is a rare monogenic subtype of migraine with aura, characterized by motor auras. The majority of FHM families have mutations in the CACNA1A and ATP1A2 genes; less than 5% of FHM families are explained by mutations in the SCN1A gene. Here we screened two Spanish FHM families for mutations in the FHM genes. Methods We assessed the clinical features of both FHM families and performed direct sequencing of all coding exons (and adjacent sequences) of the CACNA1A, ATP1A2, PRRT2 and SCN1A genes. Results FHM patients in both families had pure hemiplegic migraine with highly variable severity and frequency of attacks. We identified a novel SCN1A missense mutation p.Ile1498Met in all three tested hemiplegic migraine patients of one family. In the other family, novel SCN1A missense mutation p.Phe1661Leu was identified in six out of eight tested hemiplegic migraine patients. Both mutations affect amino acid residues that either reside in an important functional domain (in the case of Ile 1498 ) or are known to be important for kinetic properties of the Na V 1.1 channel (in the case of Phe 1661 ). Conclusions We identified two mutations in families with FHM. SCN1A mutations are an infrequent but important cause of FHM. Genetic testing is indicated in families when no mutations are found in other FHM genes.