Cerebellar atrophy - ataxia - seizures (Q94017): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed label, description and/or aliases in pt-br, en |
||
| description / pt-br | description / pt-br | ||
A ataxia autossômica recessiva devido à deficiência de ubiquinona é uma doença mitocondrial caracterizada por ataxia progressiva com início na infância e atrofia cerebelar. Intolerância ao exercício com níveis elevados de lactato e déficit intelectual leve também podem estar presentes. | |||
| description / en | description / en | ||
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. | |||
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 |
||
| 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. |
