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Absence
Antiepileptic
Autosomal dominant cortical myoclonus and epilepsy
Benign myoclonic epilepsy in infancy
Childhood absence epilepsy
Clonic
Epilepsy
Epilepsy drug
Impulsive petit mal
Mild epilepsy
Minor epilepsy
Myoclonic
Myoclonic epilepsy
Neonatal convulsions
Nonspecific epileptic seizures atonic
Petit mal
Pyknolepsy
Tonic
Tonic-clonic

Translation of "Epilepsy " (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
https://icd.who.int/browse10/2 (...) (...) [HTML]
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
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
Benign childhood epilepsy with centrotemporal EEG spikes Childhood epilepsy with occipital EEG paroxysms
https://icd.who.int/browse10/2 (...) (...) [HTML]
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
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
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
https://browser.ihtsdotools.or (...) (...) [HTML]
lissencéphalie par mutation de LIS1
SNOMEDCT-BE (disorder) / 770560008
SNOMEDCT-BE (disorder) / 770560008
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
AFG3L2 (AFG3 like matrix AAA peptidase subunit 2) related spastic ataxia, myoclonic epilepsy, neuropathy syndrome
https://browser.ihtsdotools.or (...) (...) [HTML]
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
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
petit mal | minor epilepsy
http://users.ugent.be/~rvdstic (...) (...) [HTML]
petit mal | petite crise d'épilepsie
UGENT - Medical terms -
UGENT - Medical terms -
http://users.ugent.be/~rvdstic (...) (...) [HTML]
http://users.ugent.be/~rvdstic (...) [HTML]
antiepileptic | epilepsy drug
http://users.ugent.be/~rvdstic (...) (...) [HTML]
antiépileptique (a. et s.m) | anticonvulsivant
UGENT - Medical terms -
UGENT - Medical terms -
http://users.ugent.be/~rvdstic (...) (...) [HTML]
http://users.ugent.be/~rvdstic (...) [HTML]
epilepsy
http://users.ugent.be/~rvdstic (...) (...) [HTML]
épilepsie | épilepsie
UGENT - Medical terms -
UGENT - Medical terms -
http://users.ugent.be/~rvdstic (...) (...) [HTML]
http://users.ugent.be/~rvdstic (...) [HTML]
absence | mild epilepsy
http://users.ugent.be/~rvdstic (...) (...) [HTML]
absence | absence épileptique
UGENT - Medical terms -
UGENT - Medical terms -
http://users.ugent.be/~rvdstic (...) (...) [HTML]
http://users.ugent.be/~rvdstic (...) [HTML]
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
https://browser.ihtsdotools.or (...) (...) [HTML]
syndrome de Jeavons
SNOMEDCT-BE (disorder) / 716278005
SNOMEDCT-BE (disorder) / 716278005
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Autosomal dominant cortical myoclonus and epilepsy
https://browser.ihtsdotools.or (...) (...) [HTML]
epilepsie myoclonique bénigne familiale de l'adulte
SNOMEDCT-BE (disorder) / 717225001
SNOMEDCT-BE (disorder) / 717225001
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
IN-CONTEXT TRANSLATIONS


Others have searched : benign myoclonic epilepsy in infancy    childhood absence epilepsy    nonspecific epileptic seizures atonic    absence    antiepileptic    clonic    epilepsy    epilepsy drug    impulsive petit mal    mild epilepsy    minor epilepsy    myoclonic    myoclonic epilepsy    neonatal convulsions    petit mal    pyknolepsy    tonic-clonic    Epilepsy     


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'Epilepsy '

Date index:2023-08-31 -

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