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Benign neonatal seizures

MONDO:0016027

A rare genetic epilepsy syndrome characterized by the occurrence of afebrile seizures in otherwise healthy newborns with onset in the first few days of life.

Also known as: BFNS, benign familal neonatal seizures, benign familial convulsion, benign familial convulsions, benign familial neonatal convulsions, benign familial neonatal epilepsy, benign familial neonatal seizures, seizures, benign familial neonatal

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

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Sub-types

Seizures, benign familial neonatal, 1 (0) Seizures, benign familial neonatal, 2 (0) Seizures, benign familial neonatal, 3 (0) Seizures, benign familial neonatal, autosomal recessive (0)

Broader categories

Disease (717) Epilepsy (447) Nervous system disorder (243) Hereditary disease (188) Brain disorder (131) Central nervous system disorder (115) Human disease (15) Hereditary neurological disease (6) Disease of genetic or genomic mechanism (2) Epilepsy syndrome (2)
Trials to join now! 4 Not yet finished but already full! 2 Completed 1
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