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Up to: Hereditary neurological disease · Dystonic disorder

Inherited dystonia

An instance of dystonic disorder that is caused by an inherited modification of the individual's genome.

0 trials tagged with this condition →

Combined dystonia 1 trial · 12 incl. sub-types Sub-types →
Isolated dystonia 4 trials · 11 incl. sub-types Sub-types →
Lymphatic malformation 5 8 trials
Dystonia, focal, task-specific 4 trials
Dopa-responsive dystonia due to sepiapterin reductase deficiency 1 trial
Dystonia 28, childhood-onset 1 trial
Torsion dystonia 7 1 trial
Woodhouse-Sakati syndrome 0 trials
Ataxia - oculomotor apraxia type 4 0 trials
Autosomal dominant dopa-responsive dystonia 0 trials Sub-types →
Developmental malformations-deafness-dystonia syndrome 0 trials
Dystonia 22, adult-onset 0 trials
Dystonia 22, juvenile-onset 0 trials
Dystonia 30 0 trials
Dystonia 31 0 trials
Dystonia 32 0 trials
Dystonia 33 0 trials
Dystonia 34, myoclonic 0 trials
Dystonia 35, childhood-onset 0 trials
Dystonia 37, early-onset, with striatal lesions 0 trials
Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities 0 trials
Familial idiopathic torsion dystonia 0 trials
Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome 0 trials
Striatonigral degeneration, childhood-onset 0 trials