PRRT2 links infantile convulsions and paroxysmal dyskinesia with migraine.

OBJECTIVE

Whole genome sequencing and the screening of 103 families recently led us to identify PRRT2 (proline-rich-transmembrane protein) as the gene causing infantile convulsions (IC) with paroxysmal kinesigenic dyskinesia (PKD) (PKD/IC syndrome, formerly ICCA). There is interfamilial and intrafamilial variability and the patients may have IC or PKD. Association of IC with hemiplegic migraine (HM) has also been reported. In order to explore the mutational and clinical spectra, we analyzed 34 additional families with either typical PKD/IC or PKD/IC with migraine.

METHODS

We performed Sanger sequencing of all PRRT2 coding exons and of exon-intron boundaries in the probands and in their relatives whenever appropriate.

RESULTS

Two known and 2 novel PRRT2 mutations were detected in 18 families. The p.R217Pfs8 recurrent mutation was found in ≈50% of typical PKD/IC, and the unreported p.R145Gfs31 in one more typical family. PRRT2 mutations were also found in PKD/IC with migraine: p.R217Pfs8 cosegregated with PKD associated with HM in one family, and was also detected in one IC patient having migraine with aura, in related PKD/IC familial patients having migraine without aura, and in one sporadic migraineur with abnormal MRI. Previously reported p.R240X was found in one patient with PKD with migraine without aura. The novel frameshift p.S248Afs65 was identified in a PKD/IC family member with IC and migraine with aura.

CONCLUSIONS

We extend the spectrum of PRRT2 mutations and phenotypes to HM and to other types of migraine in the context of PKD/IC, and emphasize the phenotypic pleiotropy seen in patients with PRRT2 mutations.