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

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

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]
Childhood - juvenile - absence epilepsy
https://browser.ihtsdotools.or (...) (...) [HTML]
épilepsie-absence de l'enfance
SNOMEDCT-BE (disorder) / 50866000
SNOMEDCT-BE (disorder) / 50866000
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Juvenile absence epilepsy (disorder)
https://browser.ihtsdotools.or (...) (...) [HTML]
EAJ - epilepsie, absence juvénile
SNOMEDCT-BE (disorder) / 230413002
SNOMEDCT-BE (disorder) / 230413002
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Juvenile absence epilepsy
https://browser.ihtsdotools.or (...) (...) [HTML]
epilepsie-absence juvénile
SNOMEDCT-BE (disorder) / 230413002
SNOMEDCT-BE (disorder) / 230413002
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [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]
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]
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
https://browser.ihtsdotools.or (...) (...) [HTML]
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
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
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
https://browser.ihtsdotools.or (...) (...) [HTML]
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
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [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]
Rare childhood-onset epilepsy syndrome associated with infection and a biphasic clinical course. The initial symptom is a prolonged febrile seizure on day 1 (the first phase). Afterwards, patients have variable levels of consciousness from normal to
https://browser.ihtsdotools.or (...) (...) [HTML]
encéphalopathie aigüe du lobe frontal liée à la fièvre
SNOMEDCT-BE (the first phase). Afterwards, patients have variable levels of consciousness from normal to / 766044005
SNOMEDCT-BE (disorder) / 766044005
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]


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'Childhood absence epilepsy'

Date index:2024-03-30 -

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