Autosomal recessive ataxia with oculomotor apraxia type 2 (Q96462): Difference between revisions
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Latest revision as of 12:28, 16 August 2026
Ataxia-oculomotor apraxia type 2 is a form of autosomal recessive cerebellar ataxia characterised by progressive cerebellar ataxia, axonal sensorimotor neuropathy with oculomotor apraxia, fixation instability, extrapyramidal features and an elevated serum alpha-fetoprotein level.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_907196820 |
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| English | Autosomal recessive ataxia with oculomotor apraxia type 2 |
Ataxia-oculomotor apraxia type 2 is a form of autosomal recessive cerebellar ataxia characterised by progressive cerebellar ataxia, axonal sensorimotor neuropathy with oculomotor apraxia, fixation instability, extrapyramidal features and an elevated serum alpha-fetoprotein level. |
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CID11:ID_907196820
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dki-india-ID_907196820
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Concluído
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15 August 2026
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