Autosomal recessive ataxia due to ubiquinone deficiency
What is Autosomal recessive ataxia due to ubiquinone deficiency?
This syndrome is characterised by childhood-onset progressive ataxia and cerebellar atrophy.
Other condition names
- ARCA2
- Autosomal recessive ataxia due to coenzyme Q10 deficiency
- Autosomal recessive cerebellar ataxia type 2
- Autosomal recessive spinocerebellar ataxia type 9
- SCAR9
Inheritance type
Autosomal recessive
Prevalence
- Worldwide: <1 in 1,000 000
Age of Onset
- Childhood
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on "https://www.orphadata.com". Data version 1.3.16 / 4.1.7.