SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases


In the following you will find the diseases that are treated in this facility:
Acetazolamide-responsive myotonia Acquired motor neuron disease Acquired neuromuscular junction disease Acquired skeletal muscle disease Amyotrophic lateral sclerosis Amyotrophic lateral sclerosis type 4 Andersen-Tawil syndrome Autosomal dominant proximal spinal muscular atrophy Bulbospinal muscular atrophy Cyprus facial-neuromusculoskeletal syndrome Distal hereditary motor neuropathy Distal myopathy Genetic motor neuron disease Genetic neuromuscular junction disease Genetic periodic paralysis Genetic skeletal muscle disease Hyperkalemic periodic paralysis Hypokalemic periodic paralysis Idiopathic camptocormia Idiopathic dropped head syndrome Idiopathic inflammatory myopathy Infantile-onset X-linked spinal muscular atrophy Infantile-onset ascending hereditary spastic paralysis Infectious, fungal or parasitic myopathy Intellectual disability-developmental delay-contractures syndrome Isaacs syndrome Juvenile amyotrophic lateral sclerosis Juvenile primary lateral sclerosis Macrophagic myofasciitis Madras motor neuron disease Malignant hyperthermia of anesthesia Monomelic amyotrophy Morvan syndrome Motor neuron disease Muscular channelopathy Muscular dystrophy Muscular dystrophy-white matter spongiosis syndrome Muscular tumor Myotonia fluctuans Myotonia permanens Myotonic syndrome Neurogenic scapuloperoneal syndrome, Kaeser type Neuromuscular disease Neuromuscular junction disease Non-dystrophic myopathy Paramyotonia congenita of Von Eulenburg Periodic paralysis Periodic paralysis with transient compartment-like syndrome Poliomyelitis Postpoliomyelitis syndrome Potassium-aggravated myotonia Primary lateral sclerosis Progressive muscular atrophy Proximal spinal muscular atrophy Scapuloperoneal spinal muscular atrophy Skeletal muscle disease Spinal muscular atrophy-progressive myoclonic epilepsy syndrome Tel Hashomer camptodactyly syndrome Thomsen and Becker disease Vacuolar myopathy with sarcoplasmic reticulum protein aggregates