Familial focal epilepsy with variable foci

Orpha code: 98820OMIM code: 617118

Definition

Familial focal epilepsy with variable foci is a rare genetic epilepsy disorder characterized by autosomal dominant lesional and nonlesional focal epilepsy with variable penetrance. Focal seizures emanate from different cortical locations (temporal, frontal, centroparietal, parietal, parietaloccipital, occipital) in different family members, but for each individual a single focus remains constant throughout lifetime. Seizure type (tonic, tonic-clonic or hyperkinetic) and severity varies among family members and tends to decrease (but do not disappear) during adulthood. Many patients have an aura and show automatisms during diurnal seizures whereas others have nocturnal seizures. Most individuals are of normal intelligence but patients with intellectual disability, autistic spectrum disorder and obsessive-compulsive disorder have been described.

Disease data
Classification

Disease

Synonyms
FFEVF
FFEVF
Rodzinna częściowa padaczka ze zmiennymi ogniskami
Familial partial epilepsy with variable foci
ORPHA code
98820
OMIM code
617118
ICD10 code
G40.0
ICD11 code
-

No additional description.

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