Autosomal dominant nocturnal frontal lobe epilepsy |
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CHRNA4, CHRNB2 |
Benign familial neonatal infantile seizures |
SCN2A |
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Benign familial neonatal seizures |
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KCNQ2,KCNQ3 |
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Childhood absence epilepsy |
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CLCN2 |
CACNA1H |
GABRG2 |
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Epilepsy with grand mal seizures on awakening |
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CLCN2 |
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Episodic ataxia type 1 |
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KCNA1 |
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Episodic ataxia type 2 |
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CACNA1A, CACNB4 |
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Familial hemiplegic migraine |
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CACNA1A |
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Febrile seizures |
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GABRG2 |
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Generalized epilepsy with febrile seizures plus |
SCN1A, SCN2A, SCN1B |
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GABRG2 |
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Generalized epilepsy with paroxysmal dyskinesia |
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KCNMA1 |
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Infantile spasms |
SCN1A |
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Intractable childhood epilepsy with generalized tonic-clonic seizures |
SCN1A |
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Juvenile absence epilepsy |
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CLCN2 |
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Juvenile myoclonic epilepsy |
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CLCN2 |
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GABRA1,GABRD |
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Myokymia |
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KCNQ2 |
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Severe myoclonic epilepsy of infancy |
SCN1A |
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GABRG2 |
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Spinocerebellar ataxia type 6 |
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CACNA1A |
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