Cerebellar atrophy - ataxia - seizures (Q94017): Difference between revisions
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Latest revision as of 09:07, 16 August 2026
Autosomal recessive ataxia due to ubiquinone deficiency is a mitochondrial disease characterised by childhood-onset progressive ataxia and cerebellar atrophy. Exercise intolerance with elevated lactate levels and mild intellectual deficit may also be present.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1244147456 |
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| English | Cerebellar atrophy - ataxia - seizures |
Autosomal recessive ataxia due to ubiquinone deficiency is a mitochondrial disease characterised by childhood-onset progressive ataxia and cerebellar atrophy. Exercise intolerance with elevated lactate levels and mild intellectual deficit may also be present. |
Statements
CID11:ID_1244147456
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dki-india-ID_1244147456
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Concluído
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15 August 2026
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