Early-onset ataxia with oculomotor apraxia and hypoalbuminaemia (Q94014): Difference between revisions
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CID11:ID_1071655898 | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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15 August 2026
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Latest revision as of 09:07, 16 August 2026
Ataxia with oculomotor apraxia 1 (AOA1) is a neurological disorder belonging to the group of autosomal recessive cerebellar ataxias characterised by early onset gait ataxia (between 2 and 6 years of age), dysarthria, limb dysmetria (later in disease course), oculomotor apraxia, distal and symmetric muscle weakness and wasting, mild loss of vibration and joint position sense and slow progression.
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| default for all languages | ID_1071655898 |
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| English | Early-onset ataxia with oculomotor apraxia and hypoalbuminaemia |
Ataxia with oculomotor apraxia 1 (AOA1) is a neurological disorder belonging to the group of autosomal recessive cerebellar ataxias characterised by early onset gait ataxia (between 2 and 6 years of age), dysarthria, limb dysmetria (later in disease course), oculomotor apraxia, distal and symmetric muscle weakness and wasting, mild loss of vibration and joint position sense and slow progression. |
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CID11:ID_1071655898
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dki-india-ID_1071655898
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Concluído
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15 August 2026
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