Early-onset ataxia with oculomotor apraxia and hypoalbuminaemia (Q94014)
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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.
| Language | Label | Description | Also known as |
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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. |
