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Autosomal dominant cerebellar ataxia

A clinically and genetically heterogeneous group of neurodegenerative diseases characterized by a slowly progressive ataxia of gait, stance and limbs, dysarthria and/or oculomotor disorder, due to cerebellar degeneration in the absence of coexisting diseases. The degenerative process can be limited to the cerebellum (ADCA type 3) or may additionally involve the retina (ADCA type 2), optic nerve, ponto-medullary systems, basal ganglia, cerebral cortex, spinal tracts or peripheral nerves (ADCA type 1). In ACDA type 4, a cerebellar syndrome is associated with epilepsy.

11 trials tagged with this condition →

Autosomal dominant cerebellar ataxia type I 0 trials · 16 incl. sub-types Sub-types →
Autosomal dominant cerebellar ataxia type III 0 trials · 9 incl. sub-types Sub-types →
Autosomal dominant cerebellar ataxia type IV 0 trials · 8 incl. sub-types Sub-types →
Spinocerebellar ataxia 7 7 trials
Spinocerebellar ataxia 27B, late-onset 4 trials
Spinocerebellar ataxia 9 2 trials
Spinocerebellar ataxia 27A 1 trial
GRID2-related autosomal dominant spinocerebellar ataxia 0 trials
Spinocerebellar ataxia 43 0 trials
Spinocerebellar ataxia 44 0 trials
Spinocerebellar ataxia 47 0 trials
Spinocerebellar ataxia 48 0 trials
Spinocerebellar ataxia 49 0 trials
Spinocerebellar ataxia 50 0 trials
Spinocerebellar ataxia 51 0 trials