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Absence
Antiepileptic
Asia minor country
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 "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 -




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
IN-CONTEXT TRANSLATIONS


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'minor epilepsy'

Date index:2023-12-13 -

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