MEFV gene mutations in neuro-Behçet's disease and neuro-Sweet disease.
Hidehiro IshikawaAkihiro ShindoYuichiro IiDai KishidaAtsushi NiwaYamato NishiguchiKeita MatsuuraNatsuko KatoAkane MizutaniKei TachibanaYoshinori HirataHirofumi MatsuyamaAi Ogawa-ItoAkira TaniguchiHidekazu TomimotoPublished in: Annals of clinical and translational neurology (2019)
Mediterranean fever (MEFV) gene mutations are associated with familial Mediterranean fever (FMF). Recent studies have suggested that MEFV gene mutations may act as disease modifiers in neuro-Behçet's (NBD) disease and neuro-Sweet disease (NSD). We investigated MEFV genes and clinical features in 17 patients with NBD or NSD. MEFV gene mutations were frequently observed (70.6%). Headaches and exertional leg pain were associated with MEFV gene mutations (P < 0.05). Moreover, higher frequency of white matter lesions without sites predilection (P < 0.05) and non-parenchymal lesions (P < 0.05) were also observed. MEFV gene mutations may be associated with particular findings and lesion sites.