Autosomal dominant cerebellar ataxia
MONDO:0020380A 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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Sub-types of Autosomal dominant cerebellar ataxia
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Autosomal dominant cerebellar ataxia type I 0 trials · 16 incl. sub-types
30 sub-types
- Machado-Joseph disease 11 trials Sub-types →
- Spinocerebellar ataxia type 1 10 trials
- Spinocerebellar ataxia type 2 10 trials Sub-types →
- Spinocerebellar ataxia type 8 4 trials
- Spinocerebellar ataxia type 27 2 trials
- Spinocerebellar ataxia type 23 1 trial
- Spinocerebellar ataxia type 29 1 trial
- Autosomal dominant cerebellar ataxia, deafness and narcolepsy 0 trials
- Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome 0 trials
- Cerebellar dysfunction with variable cognitive and behavioral abnormalities 0 trials
- Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism 0 trials
- Spinocerebellar ataxia 46 0 trials
- Spinocerebellar ataxia type 12 0 trials
- Spinocerebellar ataxia type 13 0 trials
- Spinocerebellar ataxia type 14 0 trials
- Spinocerebellar ataxia type 15/16 0 trials
- Spinocerebellar ataxia type 17 0 trials
- Spinocerebellar ataxia type 18 0 trials
- Spinocerebellar ataxia type 19/22 0 trials
- Spinocerebellar ataxia type 20 0 trials
- Spinocerebellar ataxia type 21 0 trials
- Spinocerebellar ataxia type 25 0 trials
- Spinocerebellar ataxia type 28 0 trials
- Spinocerebellar ataxia type 32 0 trials
- Spinocerebellar ataxia type 34 0 trials
- Spinocerebellar ataxia type 35 0 trials
- Spinocerebellar ataxia type 36 0 trials
- Spinocerebellar ataxia type 37 0 trials
- Spinocerebellar ataxia type 4 0 trials
- Spinocerebellar ataxia type 40 0 trials
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Autosomal dominant cerebellar ataxia type III 0 trials · 9 incl. sub-types
10 sub-types
- Spinocerebellar ataxia type 6 9 trials
- Spinocerebellar ataxia 45 0 trials
- Spinocerebellar ataxia type 11 0 trials
- Spinocerebellar ataxia type 26 0 trials
- Spinocerebellar ataxia type 30 0 trials
- Spinocerebellar ataxia type 31 0 trials
- Spinocerebellar ataxia type 38 0 trials
- Spinocerebellar ataxia type 41 0 trials
- Spinocerebellar ataxia type 42 0 trials Sub-types →
- Spinocerebellar ataxia type 5 0 trials
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Autosomal dominant cerebellar ataxia type IV 0 trials · 8 incl. sub-types
2 sub-types
- Dentatorubral-pallidoluysian atrophy 4 trials
- Spinocerebellar ataxia type 10 4 trials
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Spinocerebellar ataxia 7 7 trials
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Spinocerebellar ataxia 9 2 trials
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Spinocerebellar ataxia 27A 1 trial
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Spinocerebellar ataxia 43 0 trials
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Spinocerebellar ataxia 44 0 trials
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Spinocerebellar ataxia 47 0 trials
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Spinocerebellar ataxia 48 0 trials
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Spinocerebellar ataxia 49 0 trials
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Spinocerebellar ataxia 50 0 trials
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Spinocerebellar ataxia 51 0 trials