Spinocerebellar Ataxia Type 25
Description
Spinocerebellar ataxia type 25 (SCA25) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I; see this term). It is characterized by cerebellar ataxia and prominent sensory neuropathy.
Clinical Features
Top most frequent phenotypes and symptoms related to Spinocerebellar Ataxia Type 25
- Scoliosis
- Ataxia
- Nystagmus
- Strabismus
- Visual impairment
- Peripheral neuropathy
- Dysarthria
- Cerebellar atrophy
- Vomiting
- Areflexia
And another 22 symptoms. If you need more information about this disease we can help you.
Incidence and onset information
— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)— No data available about the known clinical features onset.
Alternative names
Spinocerebellar Ataxia Type 25 Is also known as sca25.
Researches and researchers
Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.Sources and references
You can check the following sources for additional information.
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