SE-ATLAS

Congenital myasthenic syndrome Intellectual disability-developmental delay-contractures syndrome Andersen-Tawil syndrome Macrophagic myofasciitis Poliomyelitis Neuromuscular disease Distal myopathy Infantile-onset X-linked spinal muscular atrophy Juvenile primary lateral sclerosis Myotonic syndrome Potassium-aggravated myotonia Bulbospinal muscular atrophy Infantile-onset ascending hereditary spastic paralysis Thomsen and Becker disease Proximal spinal muscular atrophy Periodic paralysis Muscular tumor Postpoliomyelitis syndrome Monomelic amyotrophy Cyprus facial-neuromusculoskeletal syndrome Infectious, fungal or parasitic myopathy Immune-mediated acquired neuromuscular junction disease Primary lateral sclerosis Idiopathic camptocormia Muscular dystrophy-white matter spongiosis syndrome Idiopathic dropped head syndrome Madras motor neuron disease Amyotrophic lateral sclerosis type 4 Vacuolar myopathy with sarcoplasmic reticulum protein aggregates Progressive muscular atrophy Muscular channelopathy Amyotrophic lateral sclerosis Isaacs syndrome Scapuloperoneal spinal muscular atrophy Juvenile amyotrophic lateral sclerosis Morvan syndrome Genetic skeletal muscle disease Muscular dystrophy Spinal muscular atrophy-progressive myoclonic epilepsy syndrome Paralysie périodique hypokaliémique Maladie du muscle squelettique Paralysie périodique hyperkaliémique Neuropathie motrice distale héréditaire Maladie acquise du muscle squelettique Paramyotonie d'Eulenburg Myopathie inflammatoire idiopathique Hyperthermie maligne de l'anesthésie Maladie de la jonction neuromusculaire Maladie génétique de la jonction neuromusculaire Camptodactylie de Tel Hashomer Maladie acquise de la jonction neuromusculaire Myopathies non dystrophiques Maladie du motoneurone Maladie génétique du motoneurone Myotonie permanente Myotonie fluctuante Maladie acquise du motoneurone Myotonie sensible à l'acétazolamide Botulisme Syndrome scapulo-péronier neurogénique type Kaeser Paralysie périodique avec pseudo-syndrome des loges transitoire Paralysie périodique génétique Amyotrophie spinale proximale autosomique dominante