Autosomal recessive ataxia with oculomotor apraxia type 2 (Q96462): Difference between revisions
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Ataxia-apraxia oculomotora tipo 2 é uma forma de ataxia cerebelar autossômica recessiva caracterizada por ataxia cerebelar progressiva, neuropatia sensitivo-motora axonal com apraxia oculomotora, instabilidade de fixação, características extrapiramidais e um nível elevado de alfa-fetoproteína sérica. | |||
| description / en | description / en | ||
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. | |||
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 |
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| 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. |
