spinocerebellar ataxia, autosomal recessive 3; spinocerebellar ataxia with blindness & deafness (SACR3)

Genetics

• 6p23-p21

Clinical manifestations

• features of spinocerebellar ataxia
• optic & cochlear degeneration leading to blindness & deafness

More general terms

• spinocerebellar ataxia, autosomal recessive

Database

• OMIM: https://mirror.omim.org/entry/271250