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Х-зчеплена спіноцеребеллярна атаксія, тип 4

ORPHA:85292· ICD-10 G11.1· X-linked spinocerebellar ataxia type 4

Визначення(English summary)

A rare X-linked spinocerebellar ataxia characterized by ataxia, pyramidal tract signs and adult-onset dementia. The disease manifests during early childhood with delayed walking and tremor. The pyramidal signs appear progressively and by adulthood memory problems and dementia gradually become apparent.

Поширеність
<1 / 1 000 000
Успадкування
X-linked recessive
Вік початку
Adult