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Absence
Benign myoclonic epilepsy in infancy
Childhood - juvenile - absence epilepsy
Childhood absence epilepsy
Clonic
Epilepsy with myoclonic absences
Impulsive petit mal
Juvenile absence epilepsy
Juvenile absence epilepsy
Mild epilepsy
Myoclonic
Myoclonic epilepsy
Myoclonic-astatic seizures
Neonatal convulsions
Nonspecific epileptic seizures atonic
Pyknolepsy
Tonic
Tonic-clonic

Translation of "Juvenile absence epilepsy " (English → French) :

Juvenile absence epilepsy

epilepsie-absence juvénile
SNOMEDCT-BE (disorder) / 230413002
SNOMEDCT-BE (disorder) / 230413002


Juvenile absence epilepsy (disorder)

EAJ - epilepsie, absence juvénile
SNOMEDCT-BE (disorder) / 230413002
SNOMEDCT-BE (disorder) / 230413002


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


Childhood - juvenile - absence epilepsy

épilepsie-absence de l'enfance
SNOMEDCT-BE (disorder) / 50866000
SNOMEDCT-BE (disorder) / 50866000


A rare epilepsy syndrome characterized by late-onset (after 1 year old) epileptic spasms that occur in clusters, associated with tonic seizures, atypical absences and cognitive deterioration. Language difficulties and behavior problems are frequently

spasme cryptogénique à début tardif
SNOMEDCT-BE (after 1 year old) epileptic spasms that occur in clusters, associated with tonic seizures, atypical absences and cognitive deterioration. Language difficulties and behavior problems are frequently / 778063003
SNOMEDCT-BE (disorder) / 778063003


A rare epilepsy syndrome characterised by late-onset (after 1 year old) epileptic spasms that occur in clusters, associated with tonic seizures, atypical absences and cognitive deterioration. Language difficulties and behaviour problems are frequentl

spasme infantile à début tardif
SNOMEDCT-BE (after 1 year old) epileptic spasms that occur in clusters, associated with tonic seizures, atypical absences and cognitive deterioration. Language difficulties and behavior problems are frequently / 778063003
SNOMEDCT-BE (disorder) / 778063003


absence | mild epilepsy

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


Epilepsy with:myoclonic absences | myoclonic-astatic seizures | Infantile spasms Lennox-Gastaut syndrome Salaam attacks Symptomatic early myoclonic encephalopathy West's syndrome

Encéphalopathie myoclonique précoce symptomatique Epilepsie avec:absences myocloniques | crises astato-myocloniques | Spasmes infantiles Syndrome de:Lennox-Gastaut | West | Tic de Salaam
WORLD HEALTH ORGANIZATION ICD-10: G40.4
WORLD HEALTH ORGANIZATION ICD-10: G40.4




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'Juvenile absence epilepsy'

Date index:2022-02-19 -

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