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Benign myoclonic epilepsy in infancy
Childhood absence epilepsy
Clonic
Impulsive petit mal
Myoclonic
Myoclonic epilepsy
Neonatal convulsions
Nonspecific epileptic seizures atonic
Pyknolepsy
Tonic
Tonic-clonic

Translation of "Benign myoclonic epilepsy in infancy " (English → French) :

TERMINOLOGY
see also In-Context Translations below
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

Convulsions néonatales bénignes (familiales) Crises non spécifiques:atoniques | cloniques | myocloniques | tonico-cloniques | toniques | Epilepsie (avec):absences de l'adolescence | absences de l'enfance [pyknolepsie] | crises [grand mal] au réveil | myoclonique bénigne de l'enfance | myoclonique [petit mal impulsif] juvénile
WORLD HEALTH ORGANIZATION ICD-10: G40.3
WORLD HEALTH ORGANIZATION ICD-10: G40.3
IN-CONTEXT TRANSLATIONS
‘severe myoclonic epilepsy in infancy’ (SMEI), also known as Dravet’s syndrome. This type of epilepsy

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


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.

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).


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.

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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'Benign myoclonic epilepsy in infancy'

Date index:2021-02-10 -

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