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Benign myoclonic epilepsy in infancy
Childhood absence epilepsy
Clonic
Cryptogenic epilepsy
Cryptogenic myoclonic epilepsy
Dravet syndrome
Dravet's syndrome
Epilepsy with myoclonic absences
Impulsive petit mal
Myoclonic
Myoclonic epilepsy
Myoclonic-astatic seizures
Neonatal convulsions
Nonspecific epileptic seizures atonic
Progressive myoclonic epilepsy
Pyknolepsy
SMEI
Severe myoclonic epilepsy of infancy
Tonic
Tonic-clonic

Traduction de «Cryptogenic myoclonic epilepsy » (Anglais → Néerlandais) :

Cryptogenic myoclonic epilepsy

cryptogene myoklonische epilepsie


Benign:myoclonic epilepsy in infancy | neonatal convulsions (familial) | Childhood absence epilepsy [pyknolepsy] Epilepsy with grand mal seizures on awakening Juvenile:absence epilepsy | myoclonic epilepsy [impulsive petit mal] | Nonspecific epileptic seizures:atonic | clonic | myoclonic | tonic | tonic-clonic

absence-epilepsie in kinderjaren [pyknolepsie] | benigne | infantiele myoklonische-epilepsie | benigne | neonatale convulsies (familiaal) | epilepsie met grandmalaanvallen bij ontwaken | juveniele | absence epilepsie | juveniele | myoklonische epilepsie [impulsieve petit mal] | niet-specifieke epileptische aanvallen | atonisch | niet-specifieke epileptische aanvallen | klonisch | niet-specifieke epileptische aanvallen | myoklonisch | niet-specifieke epileptische aanvallen | tonisch | niet-specifieke epileptische aanvallen | tonisch-klonisch


AFG3L2 (AFG3 like matrix AAA peptidase subunit 2) related spastic ataxia, myoclonic epilepsy, neuropathy syndrome

spastisch ataxie, myoclonische epilepsie, neuropathiesyndroom met vroege aanvang




Dravet syndrome | Dravet's syndrome | severe myoclonic epilepsy of infancy | SMEI [Abbr.]

syndroom van Dravet | SMEI [Abbr.]


Progressive myoclonic epilepsy

progressieve myoklonische epilepsie


Epilepsy with:myoclonic absences | myoclonic-astatic seizures | Infantile spasms Lennox-Gastaut syndrome Salaam attacks Symptomatic early myoclonic encephalopathy West's syndrome

epilepsie met | myoklonisch-astatische aanvallen | epilepsie met | myoklonische absences | infantiele spasmen | salaamkrampen | symptomatische myoklonische-encefalopathie, vroeg optredend | syndroom van Lennox-Gastaut | syndroom van West






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Date index: 2021-03-24
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