SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases


In the following you will find the diseases that this support group organisation focuses on:
Adult-onset cervical dystonia, DYT23 type Adult-onset dystonia-parkinsonism Ataxia-telangiectasia variant Autosomal dominant dopa-responsive dystonia Autosomal dominant focal dystonia, DYT25 type Autosomal recessive dopa-responsive dystonia Benign paroxysmal torticollis of infancy Blepharospasm-oromandibular dystonia syndrome Brain dopamine-serotonin vesicular transport disease Combined cervical dystonia Combined dystonia Cranio-cervical dystonia with laryngeal and upper-limb involvement Developmental malformations-deafness-dystonia syndrome Dopa-responsive dystonia Dopa-responsive dystonia due to sepiapterin reductase deficiency Dystonia 16 Dystonia-aphonia syndrome Early-onset generalized limb-onset dystonia Focal, segmental or multifocal dystonia Generalized isolated dystonia Hemidystonia-hemiatrophy syndrome Infantile convulsions and choreoathetosis Infantile dystonia-parkinsonism Infantile epileptic-dyskinetic encephalopathy Isolated dystonia Myoclonus-dystonia syndrome Oromandibular dystonia Paroxysmal dyskinesia Paroxysmal dystonia Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity Paroxysmal exertion-induced dyskinesia Paroxysmal kinesigenic dyskinesia Paroxysmal non-kinesigenic dyskinesia Persistent combined dystonia Primary dystonia, DYT13 type Primary dystonia, DYT17 type Primary dystonia, DYT2 type Primary dystonia, DYT21 type Primary dystonia, DYT4 type Primary dystonia, DYT6 type Rapid-onset dystonia-parkinsonism Rare disorder with dystonia and other neurologic or systemic manifestation Rare dystonia Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome Wilson disease Woodhouse-Sakati syndrome X-linked dystonia-parkinsonism