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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

Traduction de «Special epileptic syndromes » (Anglais → Français) :

Special epileptic syndromes

Syndromes épileptiques particuliers


Localization-related (focal)(partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset

Epilepsie et syndromes épileptiques idiopathiques définis par leur localisation (focale, partielle) avec crises à début focal


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

ADCME - autosomal dominant cortical myoclonus and epilepsy


Localization-related (focal)(partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures

Epilepsie et syndromes épileptiques symptomatiques définis par leur localisation (focale, partielle) avec crises partielles simples


Lennox-Gastaut syndrome | Lennox syndrome | epileptic encephalopathy with diffuse slow spike-and-wave discharges | petit mal variant

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


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


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


Landau-Kleffner syndrome [ LKS | acquired epileptic aphasia | infantile acquired aphasia ]

syndrome de Landau-Kleffner [ SLK | aphasie épileptique acquise | syndrome de Landau et Kleffner ]


Association for Children with Down Syndrome [ ACDS | Association for Special Children ]

Association for Children with Down Syndrome [ ACDS | Association for Special Children ]




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Date index: 2022-03-22
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