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Autosomal dominant cerebellar ataxia

MONDO:0020380

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.

Also known as: SCA, spinocerebellar ataxia, ADCA, Autosomal Dominant Hereditary Ataxia, autosomal dominant spinocerebellar ataxia, cerebellar ataxia, autosomal dominant, Pierre Marie cerebellar ataxia (formerly)

50 clinical trials for this condition and its sub-types, 11 tagged with Autosomal dominant cerebellar ataxia itself.

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Where it sits in the disease tree

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Part of

↑ Autosomal dominant disease (699) ↑ Hereditary dementia (322) ↑ Hereditary cerebellar ataxia (116)

Sub-types of Autosomal dominant cerebellar ataxia

Most studied deeper sub-types

Machado-Joseph disease type 3 (2) Machado-Joseph disease type 1 (0) Machado-Joseph disease type 2 (0) Machado-Joseph disease type 4 (0) Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits (0) Spinocerebellar degeneration with slow eye movements (0)
Including sub-types (50) Tagged with Autosomal dominant cerebellar ataxia (11)
Trials to join now! 2 Not yet recruiting 1 Not yet finished but already full! 7 Completed 1
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