Skip to Accessibility Menu
Skip to Login
Skip to Content
Skip to Footer
Menu
Open search
Search
Accessibility
Log in
Spinocerebellar ataxia type 32
What is Spinocerebellar ataxia type 32?
An autosomal dominant cerebellar ataxia type 1 that is characterized by ataxia and cognitive impairment. Azoospermia is a typical feature in affected males.
Other condition names
Cerebellar ataxia with azoospermia and intellectual disability
SCA32
Inheritance type
Autosomal dominant
Prevalence
Worldwide: <1 in 1,000 000
Age of Onset
Adult
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on
"https://www.orphadata.com"
. Data version 1.3.16 / 4.1.7.