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Epilepsy with myoclonic absences
Myoclonic epilepsy in non-progressive encephalopathy
Myoclonic-astatic seizures
Progressive myoclonic epilepsy

Translation of "Myoclonic epilepsy in non-progressive encephalopathy " (English → French) :

Myoclonic epilepsy in non-progressive encephalopathy

epilepsie myoclonique des encéphalopathies non-progressives
SNOMEDCT-BE (disorder) / 778047006
SNOMEDCT-BE (disorder) / 778047006


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.

epilepsie myoclonique des encéphalopathies non-progressives
SNOMEDCT-CA (trouble) / 778047006
SNOMEDCT-CA (trouble) / 778047006


Progressive myoclonic epilepsy

épilepsie myoclonique progressive
SNOMEDCT-BE (disorder) / 267581004
SNOMEDCT-BE (disorder) / 267581004


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

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
WORLD HEALTH ORGANIZATION ICD-10: G40.4


An inherited epileptic syndrome characterized by cortical hand tremors, myoclonic jerks and occasional generalized or focal seizures with a non-progressive or very slowly progressive disease course, and no signs of early dementia or cerebellar ataxia

ADCME - autosomal dominant cortical myoclonus and epilepsy
SNOMEDCT-BE (disorder) / 717225001
SNOMEDCT-BE (disorder) / 717225001




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'Myoclonic epilepsy in non-progressive encephalopathy'

Date index:2022-06-20 -

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