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Translation of "Minor epilepsy " (English → French) :
TERMINOLOGY
see also In-Context Translations below petit mal | minor epilepsy
petit mal | petite crise d'épilepsie
UGENT - Medical terms -
UGENT - Medical terms -
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
Syndrome that is characterized by the association of multiple sclerosis with lamellar ichthyosis and hematological anomalies (beta thalassemia minor and a quantitative deficit of factor VIII-von Willebrand complex). Other clinical manifestations may
syndrome de sclérose en plaques-ichtyose-déficit en facteur VIII
SNOMEDCT-BE (beta thalassemia minor and a quantitative deficit of factor VIII-von Willebrand complex). Other clinical manifestations may / 733028000
SNOMEDCT-BE (disorder) / 733028000
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
A cerebral malformation with epilepsy with predominant characteristics of posterior isolated lissencephaly with developmental delay, intellectual disability and epilepsy that usually evolves from West syndrome to Lennox-Gastaut syndrome. Additional f
lissencéphalie par mutation de LIS1
SNOMEDCT-BE (disorder) / 770560008
SNOMEDCT-BE (disorder) / 770560008
Benign childhood epilepsy with centrotemporal EEG spikes Childhood epilepsy with occipital EEG paroxysms
Epilepsie bénigne de l'enfant avec pointes-ondes centro-temporales à l'EEG [Loiseau-Beaussart] Epilepsie de l'enfant avec paroxysmes occipitaux à l'EEG
WORLD HEALTH ORGANIZATION ICD-10: G40.0
WORLD HEALTH ORGANIZATION ICD-10: G40.0
absence | mild epilepsy
absence | absence épileptique
UGENT - Medical terms -
UGENT - Medical terms -
epilepsy
épilepsie | épilepsie
UGENT - Medical terms -
UGENT - Medical terms -
antiepileptic | epilepsy drug
antiépileptique (a. et s.m) | anticonvulsivant
UGENT - Medical terms -
UGENT - Medical terms -
Asia minor country
pays du sous-continent indien
SNOMEDCT-BE (geographic location) / 223596000
SNOMEDCT-BE (geographic location) / 223596000
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'Minor epilepsy'
Date index:2022-02-09 -
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