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

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Encéphalopathie myoclonique précoce symptomatique Epilepsie avec:absences myocloniques | crises astato-myocloniques | Spasmes infantiles Syndrome de:Lennox-Gastaut | West | Tic de Salaam

WORLD HEALTH ORGANIZATION ICD-10: G40.4

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A rare epilepsy syndrome with characteristics of recurrent, long-lasting myoclonic status in infants and young children with a non-progressive encephalopathy, associated with transient and recurring motor, cognitive and/or behavioral disturbances.

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epilepsie myoclonique des encéphalopathies non-progressives

SNOMEDCT-CA (trouble) / 778047006

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A cerebral malformation with epilepsy with predominant characteristics of posterior isolated lissencephaly with developmental delay, intellectual disability and epilepsy that usually evolves from West syndrome to Lennox-Gastaut syndrome. Additional f

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lissencéphalie par mutation de LIS1

SNOMEDCT-BE (disorder) / 770560008

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Benign childhood epilepsy with centrotemporal EEG spikes Childhood epilepsy with occipital EEG paroxysms

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Epilepsie bénigne de l'enfant avec pointes-ondes centro-temporales à l'EEG [Loiseau-Beaussart] Epilepsie de l'enfant avec paroxysmes occipitaux à l'EEG

WORLD HEALTH ORGANIZATION ICD-10: G40.0

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A rare chromosomal anomaly syndrome resulting from a partial interstitial deletion of the short arm of chromosome 9. The disease has characteristics of mild to moderate developmental delay, hand tremors, myoclonic jerks, attention deficit-hyperactivi

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syndrome de microdélétion 9p13

SNOMEDCT-BE (disorder) / 764725008

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Early myoclonic encephalopathy

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encéphalopathie myoclonique précoce

SNOMEDCT-BE (disorder) / 44423001

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IN-CONTEXT TRANSLATIONS

‘severe myoclonic epilepsy in infancy’ (SMEI), also known as Dravet’s syndrome. This type of epilepsy

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d’épilepsie appelée «épilepsie myoclonique sévère du nourrisson» (EMSN), également connue sous le

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It is used in conjunction with clobazam and valproate to treat a certain form of epilepsy called severe myoclonic epilepsy in infancy (Dravet’s syndrome), which affects children.

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Il est utilisé en association au clobazam et au valproate pour le traitement d’une forme d’épilepsie qui atteint des enfants, appelée épilepsie myoclonique sévère du nourrisson (syndrome de Dravet).

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Diacomit is indicated for use in conjunction with clobazam and valproate as adjunctive therapy of refractory generalized tonic-clonic seizures in patients with severe myoclonic epilepsy in infancy (SMEI, Dravet’s syndrome) whose seizures are not adequately controlled with clobazam and valproate.

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Diacomit est indiqué en association au valproate de sodium et au clobazam dans le traitement des convulsions tonicocloniques généralisées chez des patients atteints d’une épilepsie myoclonique sévère du nourrisson (EMSN, syndrome de Dravet) et insuffisamment contrôlées par l’association clobazam/valproate de sodium.

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Others have searched : benign myoclonic epilepsy in infancy childhood absence epilepsy early myoclonic encephalopathy epilepsy with myoclonic absences myoclonic epilepsy in non-progressive encephalopathy nonspecific epileptic seizures atonic progressive myoclonic epilepsy clonic impulsive petit mal myoclonic myoclonic epilepsy myoclonic-astatic seizures neonatal convulsions pyknolepsy tonic-clonic Myoclonic epilepsy

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'Myoclonic epilepsy'

Date index:2023-06-02 -

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Translation of "Myoclonic epilepsy " (English → French) :

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