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Familial partial epilepsy

MONDO:0017704

An instance of partial epilepsy that is caused by an inherited modification of the individual's genome.

Also known as: familial focal epilepsy, hereditary partial epilepsy, epilepsy, partial, familial

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

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Sub-types

Temporal lobe epilepsy (29) Mesial temporal lobe epilepsy with hippocampal sclerosis (10) Self-limited epilepsy with centrotemporal spikes (3) Generalized epilepsy-paroxysmal dyskinesia syndrome (1) Autosomal dominant epilepsy with auditory features (0) Autosomal dominant nocturnal frontal lobe epilepsy 1 (0) Autosomal dominant nocturnal frontal lobe epilepsy 2 (0) Autosomal dominant nocturnal frontal lobe epilepsy 3 (0) Autosomal dominant nocturnal frontal lobe epilepsy 4 (0) Autosomal dominant nocturnal frontal lobe epilepsy 5 (0) Epilepsy, familial focal, with variable foci 1 (0) Epilepsy, familial focal, with variable foci 2 (0) Epilepsy, familial focal, with variable foci 3 (0) Epilepsy, familial focal, with variable foci 4 (0) Epilepsy, familial temporal lobe, 1 (0) Familial focal epilepsy with variable foci (0) Familial mesial temporal lobe epilepsy (0) Familial sleep-related hypermotor epilepsy (0) Familial temporal lobe epilepsy 2 (0) Familial temporal lobe epilepsy 3 (0)

Broader categories

Disease (618) Epilepsy (398) Nervous system disorder (217) Hereditary disease (172) Brain disorder (110) Central nervous system disorder (97) Focal epilepsy (91) Childhood-onset epilepsy syndrome (16) Human disease (14) Hereditary neurological disease (5)
Trials to join now! 25 Not yet recruiting 5 Not yet finished but already full! 8 Completed 4 Terminated 2
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