A rare Huntington disease-like syndrome with characteristics of childhood-onset progressive neurologic deterioration with pyramidal and extrapyramidal abnormalities, chorea, dystonia, ataxia, gait instability, spasticity, seizures, mutism, and (on br

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maladie de Huntington-like 3

SNOMEDCT-BE (on br / 770939009

SNOMEDCT-BE (disorder) / 770939009

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Benign hereditary chorea

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chorée bénigne héréditaire

SNOMEDCT-BE (disorder) / 230306001

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Chorea (finding)

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chorée

SNOMEDCT-BE (finding) / 271700006

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Post-hemiplegic chorea

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chorée posthémiplégique

SNOMEDCT-BE (disorder) / 76628006

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Drug-induced chorea

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Chorée médicamenteuse

WORLD HEALTH ORGANIZATION ICD-10: G25.4

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Definition: A dementia occurring as part of a widespread degeneration of the brain. The disorder is transmitted by a single autosomal dominant gene. Symptoms typically emerge in the third and fourth decade. Progression is slow, leading to death usually within 10 to 15 years. | Dementia in Huntington's chorea

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Définition: Démence survenant dans le contexte d'une dégénérescence cérébrale étendue. La maladie est transmise par un gène autosomique dominant unique. Les symptômes apparaissent typiquement dans la troisième et la quatrième décennies. L'évolution est lentement progressive, aboutissant habituellement à la mort en 10 à 15 années. | Démence de la chorée de Huntington

WORLD HEALTH ORGANIZATION ICD-10: F02.2*

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Senile chorea

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chorée non héréditaire progressive chronique

SNOMEDCT-BE (disorder) / 3456001

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Huntington chorea

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maladie de Huntington