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AIDP
Acute autoimmune neuropathy
Acute idiopathic facial neuropathy
Acute idiopathic polyneuritis
Acute idiopathic polyradiculoneuritis
Acute inflammatory demyelinating polyneuropathy
Acute inflammatory polyneuropathy
Acute inflammatory polyradiculoneuropathy
Bell palsy
Bell's palsy
Benign myoclonic epilepsy in infancy
Blitz-Nick-Salaam-Krämpfe
Childhood absence epilepsy
Clonic
Cryptogenic epilepsy
Eclampsia nutans
Epilepsy syndrome
Flexion spasm
GBS
Generalized flexion epilepsy syndrome
Generalized idiopathic epilepsy and epileptic syndromes
Guillain-Barré syndrome
Guillain-Barré-Strohl syndrome
Herpetic facial paralysis
IGE
Idiopathic atrophoderma Pasini-Pierini
Idiopathic epilepsy
Idiopathic facial paralysis
Idiopathic generalised epilepsies
Idiopathic generalised epilepsy
Impulsive petit mal
Infantile spasm
Infantile spastic epilepsy
Infectious polyneuritis
Jackknife spa
LGBS
Landry's paralysis
Landry-Guillain-Barré Syndrome
Myoclonic
Myoclonic epilepsy
Neonatal convulsions
Nodding spasm
Nonspecific epileptic seizures atonic
PGE
Primary generalised epilepsy
Progressive idiopathic atrophoderma
Pyknolepsy
Salaam attack
Salaam convulsion
Salaam seizure
Tonic
Tonic-clonic
West syndrome

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

TERMINOLOGY
see also In-Context Translations below
idiopathic epilepsy [ cryptogenic epilepsy ]

épilepsie idiopathique [ épilepsie cryptogénétique ]
Nervous System
Système nerveux


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


idiopathic generalised epilepsies | idiopathic generalised epilepsy | primary generalised epilepsy | IGE [Abbr.] | PGE [Abbr.]

épilepsie généralisée idiopathique
IATE - Health
IATE - Health


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)


Jeavons syndrome is an idiopathic generalised form of reflex epilepsy characterised by childhood onset, unique seizure manifestations, striking light sensitivity, and possible occurrence of generalised tonic-clonic seizures. Onset occurs in childhood

syndrome de Jeavons
SNOMEDCT-BE (disorder) / 716278005
SNOMEDCT-BE (disorder) / 716278005


acute autoimmune neuropathy | acute idiopathic polyneuritis | acute idiopathic polyradiculoneuritis | acute inflammatory demyelinating polyneuropathy | acute inflammatory demyelinating polyradiculoneuropathy | acute inflammatory polyneuropathy | acute inflammatory polyradiculoneuropathy | Guillain-Barré syndrome | Guillain-Barré-Strohl syndrome | infectious polyneuritis | Landry-Guillain-Barré Syndrome | Landry's paralysis | AIDP [Abbr.] | GBS [Abbr.] | LGBS [Abbr.]

polyradiculonévrite aiguë | polyradiculonévrite aiguë inflammatoire | polyradiculonévrite curable | syndrome de Guillain-Barré
IATE - Health
IATE - Health


Bell palsy [ Bell's palsy | idiopathic facial paralysis | herpetic facial paralysis | acute idiopathic facial neuropathy ]

paralysie de Bell [ maladie de Bell | paralysie faciale a frigore | paralysie faciale idiopathique | paralysie faciale essentielle | paralysie faciale périphérique ]
Nervous System | Human Diseases - Various
Système nerveux | Maladies humaines diverses


idiopathic atrophoderma Pasini-Pierini | progressive idiopathic atrophoderma

atrophodermie progressive idiopathique | atrophodermie progressive idiopathique de Pasini-Pierini
IATE - Health
IATE - Health


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
Epilepsy can be separated into two types: idiopathic epilepsy and symptomatic epilepsy.

Il existe deux types d'épilepsie: l'épilepsie idiopathique et l'épilepsie symptomatique.


This condition can be separated into two types, idiopathic epilepsy and symptomatic epilepsy.

Il existe deux types d'épilepsie: l'épilepsie idiopathique et l'épilepsie symptomatique.


Levetiracetam || Keppra || 2007/ 2009 || Extension of the indication to include adjunctive therapy in the treatment of primary generalised tonic-clonic (PGTC) seizures in adults and adolescents from 12 years of age with idiopathic generalised epilepsy; Extension of indication to include the adjunctive treatment of partial seizures with or without secondary generalisation in children from 1 month to

Lévétiracétam || Keppra || 2007/ 2009 || Extension de l’indication pour inclure la thérapie adjonctive dans le traitement des crises partielles avec généralisation primaire chez les adultes et les adolescents à partir de 12 ans atteints d’épilepsie généralisée idiopathique Extension de l’indication pour inclure le traitement adjonctif des crises partielles avec ou sans généralisation secondaire chez les enfants de 1 mois à


Levetiracetam || Keppra || 2007/ 2009 || Extension of the indication to include adjunctive therapy in the treatment of primary generalised tonic-clonic (PGTC) seizures in adults and adolescents from 12 years of age with idiopathic generalised epilepsy; Extension of indication to include the adjunctive treatment of partial seizures with or without secondary generalisation in children from 1 month to

Lévétiracétam || Keppra || 2007/ 2009 || Extension de l’indication pour inclure la thérapie adjonctive dans le traitement des crises partielles avec généralisation primaire chez les adultes et les adolescents à partir de 12 ans atteints d’épilepsie généralisée idiopathique Extension de l’indication pour inclure le traitement adjonctif des crises partielles avec ou sans généralisation secondaire chez les enfants de 1 mois à




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'Idiopathic epilepsy'

Date index:2023-07-19 -

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