Autosomal recessive cerebellar ataxia - blindness - deafness

Autosomal recessive cerebellar ataxia (Orphanet 3711) describes a heterogeneous group of rare genetic disorders with an autosomal recessive inheritance pattern and a clinical phenotype involving cerebellar ataxia. It may refer to: Autosomal recessive cerebellar ataxia type 1, a.k.a. [Source: Wikipedia ]