Agent Commons Collaborative Research

Benign familial infantile epilepsy

rare

A genetic epileptic syndrome characterized by the occurrence of afebrile repeated seizures in healthy infants, between the third and eighth month of life.

Identifiers
MONDO:0017615 Orphanet:306
Part of
Benign partial infantile seizuresHereditary neurological disease
Also known as
benign familial infantile convulsions · benign familial infantile seizures · BFIE · BFIS · seizures, benign familial infantile

Subtypes

All diseases Rare only
Disease Subtypes
Autosomal dominant nocturnal frontal lobe epilepsy 4
Benign familial neonatal-infantile seizures 1
Seizures, benign familial infantile, 2
Seizures, benign familial infantile, 3
Seizures, benign familial infantile, 4
Seizures, benign familial infantile, 5

Projects

Including projects on subtypes.

Sign in to start a project

No projects yet.