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Absence
Antiepileptic
Assist in epilepsy surgery
Blitz-Nick-Salaam-Krämpfe
Eclampsia nutans
Epilepsy
Epilepsy drug
Epilepsy syndrome
Flexion spasm
Generalized flexion epilepsy syndrome
Infantile spasm
Infantile spastic epilepsy
Jackknife spa
Mild disability
Mild epilepsy
Mild handicap
Mild impairment
Minor disability
Minor handicap
Minor impairment
Nodding spasm
Salaam attack
Salaam convulsion
Salaam seizure
Serve in epilepsy surgeries
Serve in epilepsy surgery
Support in epilepsy surgeries
West syndrome

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

TERMINOLOGY
see also In-Context Translations below
absence | mild epilepsy

absence | absence épileptique
UGENT - Medical terms -
UGENT - Medical terms -


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 genetic epilepsy characterized by relatively large head circumference or macrocephaly, diminished or absent deep-tendon reflexes and mild gross motor delay in infancy, followed by intractable focal seizures with language regression, behavioral

syndrome de dysplasie corticale-épilepsie focale
SNOMEDCT-BE (disorder) / 771142009
SNOMEDCT-BE (disorder) / 771142009


A rare chromosomal anomaly with characteristics of developmental delay, mild to moderate intellectual disability, epilepsy, and unspecific dysmorphic signs. High palate, delayed permanent tooth eruption, hypoplastic fingernails, clinodactyly and shor

syndrome de microdélétion 20p13
SNOMEDCT-BE (disorder) / 773346008
SNOMEDCT-BE (disorder) / 773346008


A rare infantile epilepsy syndrome characterized by complex partial seizures presenting with motion arrest, decreased responsiveness, staring, automatisms and mild clonic movements, with or without apnea, normal interictal EEG and focal, mostly tempo

epilepsie bénigne partielle de l'enfant avec crises partielles complexes
SNOMEDCT-BE (disorder) / 770624005
SNOMEDCT-BE (disorder) / 770624005


major depressive disorder, recurrent episode, mild [ major depressive disorder, recurrent, mild | major depression, recurrent, mild ]

trouble dépressif caractérisé, épisode récurrent, léger [ trouble dépressif majeur, récurrent, léger | dépression majeure, récurrente, légère ]
Neuroses | Clinical Psychology
Névroses | Psychologie clinique


mild disability [ mild impairment | minor disability | minor impairment | minor handicap | mild handicap ]

déficience légère [ déficience mineure | handicap léger | handicap mineur ]
Sociology of persons with a disability
Sociologie des personnes handicapées


serve in epilepsy surgeries | support in epilepsy surgeries | assist in epilepsy surgery | serve in epilepsy surgery

assister un chirurgien pendant une intervention pour épilepsie
skill
Aptitude


antiepileptic | epilepsy drug

antiépileptique (a. et s.m) | anticonvulsivant
UGENT - Medical terms -
UGENT - Medical terms -


epilepsy

épilepsie | épilepsie
UGENT - Medical terms -
UGENT - Medical terms -
IN-CONTEXT TRANSLATIONS
Epilepsy is characterized by sudden, brief, recurring seizures that range from mild to severe and which may cause loss of consciousness.

L'épilepsie se caractérise par des crises soudaines, brèves et récurrentes qui peuvent être plus ou moins graves et entraîner une perte de conscience.




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'Mild epilepsy'

Date index:2022-10-24 -

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