SE-ATLAS

Early-onset generalized limb-onset dystonia Oromandibular dystonia Combined dystonia Wilson disease Cranio-cervical dystonia with laryngeal and upper-limb involvement Primary dystonia, DYT17 type Dystonia-aphonia syndrome Primary dystonia, DYT21 type Rare disorder with dystonia and other neurologic or systemic manifestation Woodhouse-Sakati syndrome Paroxysmal dystonia Myoclonus-dystonia syndrome Primary dystonia, DYT2 type X-linked dystonia-parkinsonism Infantile epileptic-dyskinetic encephalopathy Isolated dystonia Primary dystonia, DYT13 type Focal, segmental or multifocal dystonia Primary dystonia, DYT6 type Primary dystonia, DYT4 type Blepharospasm-oromandibular dystonia syndrome Paroxysmal kinesigenic dyskinesia Autosomal dominant dopa-responsive dystonia Hemidystonia-hemiatrophy syndrome Paroxysmal exertion-induced dyskinesia Combined cervical dystonia Paroxysmal non-kinesigenic dyskinesia Dopa-responsive dystonia due to sepiapterin reductase deficiency Infantile dystonia-parkinsonism Adult-onset cervical dystonia, DYT23 type Adult-onset dystonia-parkinsonism Dystonia 16 Benign paroxysmal torticollis of infancy Brain dopamine-serotonin vesicular transport disease Rapid-onset dystonia-parkinsonism Rare dystonia Infantile convulsions and choreoathetosis Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity Persistent combined dystonia Entwicklungsdefekte-Schwerhörigkeit-Dystonie-Syndrom Dyskinesie, paroxysmale Generalisierte isolierte Dystonie Ataxia-Teleangiectasia Variante Dystonie, fokale, autosomal-dominante, Typ DYT25 Dopa-sensitive Dystonie Dopa-responsive Dystonie, autosomal-rezessive Schwere motorische und intellektuelle Beeinträchtigung-sensorinsorineurale Schwerhörigkeit-Dystonie-Syndrom