Harding ataxia (Q106305): Difference between revisions
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Ataxia cerebelar de inicio precoce com reflexos tendinosos preservados, ou ataxia de Harding, é um transtorno neurológico que pertence ao grupo de ataxias cerebelares autossômicos recessivos. É um transtorno heterogêneo caracterizado por ataxia cerebelar de início precoce na primeira ou segunda década de vida e há preservação dos reflexos tendinosos profundos. | |||
| description / en | description / en | ||
Early onset cerebellar ataxia with retained tendon reflexes or Harding ataxia is a neurological disorder belonging to the group of autosomal recessive cerebellar ataxias. It is a heterogeneous disorder characterised by early onset cerebellar ataxia in the first or second decade and preservation of deep tendon reflexes. | |||
Revision as of 13:13, 17 August 2026
Early onset cerebellar ataxia with retained tendon reflexes or Harding ataxia is a neurological disorder belonging to the group of autosomal recessive cerebellar ataxias. It is a heterogeneous disorder characterised by early onset cerebellar ataxia in the first or second decade and preservation of deep tendon reflexes.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1712796818 |
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| English | Harding ataxia |
Early onset cerebellar ataxia with retained tendon reflexes or Harding ataxia is a neurological disorder belonging to the group of autosomal recessive cerebellar ataxias. It is a heterogeneous disorder characterised by early onset cerebellar ataxia in the first or second decade and preservation of deep tendon reflexes. |
