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Blitz-Nick-Salaam-Krämpfe
Eclampsia nutans
Epilepsy syndrome
Flexion spasm
Generalized flexion epilepsy syndrome
Generalized idiopathic epilepsy and epileptic syndromes
Infantile spasm
Infantile spastic epilepsy
Jackknife spa
Nodding spasm
Other generalized epilepsy and epileptic syndromes
Salaam attack
Salaam convulsion
Salaam seizure
West syndrome

Translation of "Generalized idiopathic epilepsy and epileptic syndromes " (English → French) :

Generalized idiopathic epilepsy and epileptic syndromes

Epilepsie et syndromes épileptiques généralisés idiopathiques
WORLD HEALTH ORGANIZATION ICD-10: G40.3
WORLD HEALTH ORGANIZATION ICD-10: G40.3


Localization-related (focal)(partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset

Epilepsie et syndromes épileptiques idiopathiques définis par leur localisation (focale, partielle) avec crises à début focal
WORLD HEALTH ORGANIZATION ICD-10: G40.0
WORLD HEALTH ORGANIZATION ICD-10: G40.0


Other generalized epilepsy and epileptic syndromes

Autres épilepsies et syndromes épileptiques généralisés
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


infantile spasm [ West syndrome | nodding spasm | salaam convulsion | salaam seizure | salaam attack | generalized flexion epilepsy syndrome | epilepsy syndrome | Blitz-Nick-Salaam-Krämpfe | eclampsia nutans | flexion spasm | infantile spastic epilepsy | infantile spastic epilepsy | jackknife spa ]

spasme infantile [ syndrome de West | spasme en flexion | tic de salaam | syndrome des spasmes en flexion | épilepsie en flexion généralisée | encéphalite myoclonique infantile avec hypsarythmie | spasmus nutans ]
Nervous System | Symptoms (Medicine)
Système nerveux | Symptômes (Médecine)


A rare epilepsy syndrome characterised by late-onset (after 1 year old) epileptic spasms that occur in clusters, associated with tonic seizures, atypical absences and cognitive deterioration. Language difficulties and behaviour problems are frequentl

spasme infantile à début tardif
SNOMEDCT-BE (after 1 year old) epileptic spasms that occur in clusters, associated with tonic seizures, atypical absences and cognitive deterioration. Language difficulties and behavior problems are frequently / 778063003
SNOMEDCT-BE (disorder) / 778063003


A rare epilepsy syndrome characterized by late-onset (after 1 year old) epileptic spasms that occur in clusters, associated with tonic seizures, atypical absences and cognitive deterioration. Language difficulties and behavior problems are frequently

spasme cryptogénique à début tardif
SNOMEDCT-BE (after 1 year old) epileptic spasms that occur in clusters, associated with tonic seizures, atypical absences and cognitive deterioration. Language difficulties and behavior problems are frequently / 778063003
SNOMEDCT-BE (disorder) / 778063003




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'Generalized idiopathic epilepsy and epileptic syndromes'

Date index:2021-06-13 -

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