X-linked spinocerebellar ataxia type 4

Orpha code: 85292OMIM code: 301840

Definition

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.

Disease data
Classification

Disease

Synonyms
SCAX4
SCAX4
Zespół ataksja-demencja sprzężony z chromosem X
X-linked ataxia-dementia syndrome
ORPHA code
85292
OMIM code
301840
ICD10 code
G11.1
ICD11 code
-

No additional description.

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