dystonia
human disease
dopamine-responsive dystonia
genetic movement disorder
X-linked dystonia-parkinsonism
focal dystonia characterized by parkinsonism that is frequently accompanied by focal dystonia and progresses to generalized dystonia that has material basis in an SVA retrotransposon insertion in the intron of the TAF1 gene on chromosome Xq13.1
torticollis
dystonic condition defined by an abnormal, asymmetrical head or neck position, which may be due to a variety of causes
infantile parkinsonism-dystonia
Infantile dystonia-parkinsonism (IPD) is an extremely rare inherited neurological syndrome that presents in early infancy with hypokinetic parkinsonism and dystonia and that can be fatal
focal dystonia
dystonia that is localized to a specific part of the body
myoclonic dystonia
dystonia characterized by myoclonic jerks affecting mostly proximal muscles and dystonia, usually torticollis or writer's cramp, that typically responds to alcohol and has onset in the first of second decade of life