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Autosomal dominant cerebellar ataxia type I

Autosomal dominant cerebellar ataxia (ADCA) type I is a group of spinocerebellar ataxias (SCAs) characterized by ataxia with other neurological signs, including oculomotor disturbances, cognitive deficits, pyramidal and extrapyramidal dysfunction, bulbar, spinal and peripheral nervous system involvement.

0 trials tagged with this condition →

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