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ACDS
Acquired epileptic aphasia
Association for Children with Down Syndrome
Association for Special Children
Infantile acquired aphasia
LKS
Landau-Kleffner syndrome
Lennox syndrome
Lennox-Gastaut syndrome
Petit mal variant
Special epileptic syndromes

Translation of "Special epileptic syndromes " (English → French) :

Special epileptic syndromes
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Syndromes épileptiques particuliers
WORLD HEALTH ORGANIZATION ICD-10: G40.5
WORLD HEALTH ORGANIZATION ICD-10: G40.5
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
Localization-related (focal)(partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Epilepsie et syndromes épileptiques idiopathiques définis par leur localisation (focale, partielle) avec crises à début focal
WORLD HEALTH ORGANIZATION ICD-10: G40.0
WORLD HEALTH ORGANIZATION ICD-10: G40.0
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
An inherited epileptic syndrome characterized by cortical hand tremors, myoclonic jerks and occasional generalized or focal seizures with a non-progressive or very slowly progressive disease course, and no signs of early dementia or cerebellar ataxia
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
ADCME - autosomal dominant cortical myoclonus and epilepsy
SNOMEDCT-BE (disorder) / 717225001
SNOMEDCT-BE (disorder) / 717225001
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Localization-related (focal)(partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Epilepsie et syndromes épileptiques symptomatiques définis par leur localisation (focale, partielle) avec crises partielles simples
WORLD HEALTH ORGANIZATION ICD-10: G40.1
WORLD HEALTH ORGANIZATION ICD-10: G40.1
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
Lennox-Gastaut syndrome | Lennox syndrome | epileptic encephalopathy with diffuse slow spike-and-wave discharges | petit mal variant
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
syndrome de Lennox-Gastaut | SLG | syndrome de Lennox | maladie de Gastaut | encéphalopathie épileptique avec pointes-ondes lentes diffuses | encéphalopathie épileptique de l'enfant avec pointes-ondes lentes diffuses | épilepsie myokinétique grave de la première enfance avec pointes-ondes lentes | variante de petit mal | petit mal variant
médecine > sémiologie et pathologie | médecine > neurologie
médecine > sémiologie et pathologie | médecine > neurologie
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]
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] [2018-01-01]
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] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
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] [2018-01-01]
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] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Landau-Kleffner syndrome [ LKS | acquired epileptic aphasia | infantile acquired aphasia ]
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
syndrome de Landau-Kleffner [ SLK | aphasie épileptique acquise | syndrome de Landau et Kleffner ]
Nervous System | Human Diseases - Various
Système nerveux | Maladies humaines diverses
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]
Association for Children with Down Syndrome [ ACDS | Association for Special Children ]
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
Association for Children with Down Syndrome [ ACDS | Association for Special Children ]
Organizations, Administrative Units and Committees
Organismes, unités administratives et comités
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]


Others have searched : association for special children    landau-kleffner syndrome    lennox syndrome    lennox-gastaut syndrome    special epileptic syndromes    acquired epileptic aphasia    infantile acquired aphasia    petit mal variant    Special epileptic syndromes    


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'Special epileptic syndromes'

Date index:2023-09-16 -

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