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Benign myoclonic epilepsy in infancy
Childhood absence epilepsy
Clonic
Early myoclonic encephalopathy
Epilepsy with myoclonic absences
Impulsive petit mal
Myoclonic
Myoclonic epilepsy
Myoclonic epilepsy in non-progressive encephalopathy
Myoclonic-astatic seizures
Neonatal convulsions
Nonspecific epileptic seizures atonic
Progressive myoclonic epilepsy
Pyknolepsy
Tonic
Tonic-clonic

Translation of "Myoclonic " (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


Myoclonic epilepsy in non-progressive encephalopathy

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


Early myoclonic encephalopathy

encéphalopathie myoclonique précoce
SNOMEDCT-BE (disorder) / 44423001
SNOMEDCT-BE (disorder) / 44423001


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


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

syndrome d'ataxie spastique-epilepsie myoclonique-neuropathie précoce
SNOMEDCT-BE (AFG3 like matrix AAA peptidase subunit 2) related spastic ataxia, myoclonic epilepsy, neuropathy syndrome / 771469002
SNOMEDCT-BE (disorder) / 771469002


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


Syndrome with characteristics of episodes of myoclonus. Renal disease is an inconsistent feature occuring in some but not all cases. Myoclonic jerks typically occur in the torso, upper and lower limbs and face. Some affected individuals develop seizu

syndrome de myoclonus d'action-insuffisance rénale
SNOMEDCT-BE (disorder) / 764453009
SNOMEDCT-BE (disorder) / 764453009


Progressive myoclonic epilepsy

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


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

syndrome de microdélétion 9p13
SNOMEDCT-BE (disorder) / 764725008
SNOMEDCT-BE (disorder) / 764725008


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
IN-CONTEXT TRANSLATIONS


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'Myoclonic'

Date index:2023-08-25 -

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