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References OMIM Gene GeneReviews HGMD HGNC
last update : 28-06-2017
Symbol FFEVF3
Location 16p13.3
Name familial focal epilepsy with variable foci, 3
Corresponding gene NPRL3
Main clinical features
  • focal seizures arising from different cortical regions, including the temporal, frontal, parietal, and occipital lobes
  • seizure types commonly include temporal lobe epilepsy (TLE), frontal lobe epilepsy (FLE), and nocturnal frontal lobe epilepsy (NFLE)
  • any patients have structural brain abnormalities, particularly focal cortical dysplasia (FCD)
  • Genetic determination autosomal dominant
    Function/system disorder neurology
    Type disease