Autosomal recessive spastic ataxia of Charlevoix-Saguenay (Q96470): Difference between revisions
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Ataxia espástica autossômica recessiva de Charlevoix-Saguenay é um transtorno neurodegenerativo caracterizado por ataxia cerebelar de início precoce com espasticidade, uma síndrome piramidal e neuropatia periférica. | |||
| description / en | description / en | ||
Autosomal recessive spastic ataxia of Charlevoix-Saguenay is a neurodegenerative disorder characterised by early-onset cerebellar ataxia with spasticity, a pyramidal syndrome and peripheral neuropathy. | |||
Revision as of 12:28, 16 August 2026
Autosomal recessive spastic ataxia of Charlevoix-Saguenay is a neurodegenerative disorder characterised by early-onset cerebellar ataxia with spasticity, a pyramidal syndrome and peripheral neuropathy.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_345074673 |
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| English | Autosomal recessive spastic ataxia of Charlevoix-Saguenay |
Autosomal recessive spastic ataxia of Charlevoix-Saguenay is a neurodegenerative disorder characterised by early-onset cerebellar ataxia with spasticity, a pyramidal syndrome and peripheral neuropathy. |
