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Benign familial infantile epilepsy

MONDO:0017615

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

Also known as: BFIE, BFIS, benign familial infantile convulsions, benign familial infantile seizures, seizures, benign familial infantile

6 clinical trials for this condition and its sub-types.

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Sub-types

Benign familial neonatal-infantile seizures 1 (0) Seizures, benign familial infantile, 2 (0) Seizures, benign familial infantile, 3 (0) Seizures, benign familial infantile, 4 (0) Seizures, benign familial infantile, 5 (0)

Broader categories

Disease (618) Epilepsy (398) Nervous system disorder (217) Hereditary disease (172) Brain disorder (110) Central nervous system disorder (97) Human disease (14) Hereditary neurological disease (5) Disease of genetic or genomic mechanism (2) Epilepsy syndrome (2)
Trials to join now! 3 Not yet finished but already full! 3
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