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Differential Diagnosis For Cholinergic crisis/toxidrome - Causes, EMG/Abnormal findings: Hereditary, Familial, Genetic Disorders


List of current finding(s):

Hereditary, Familial, Genetic Disorders: next: Degenerative-Age Related Causes
Duchenne's Muscular Dystrophy/Pseudohypertrophic
Erb's Muscular Dystrophy/Limb Girdle MD
Muscular dystrophy
Muscular dystrophy, limb girdle type
Muscular dystrophy, progressive
Spinal muscle atrophy
Spinal muscle atrophy, infantile
Juvenile spinal muscle atrophy (Kugelberg-Welander)
Kennedy Muscular atrophy disease
Mitochondrial myopathy/MERRF
Myhre Syndrome
Potassium-Aggravated Myotonia
Distal muscular dystrophy (Gowers)
Facioscapulohumeral muscular dystrophy
Kearns-Sayre Ophthalmoplegic Syndrome
Muscular atrophy, infantile, spinal
Myotonia atrophica (Steinert's disease)
Myotonia congenita (Thomsens d.)
Nemaline myopathy
Oculopharyngeal muscular dystrophy
Progressive spinal muscular atrophy
Spinal muscle atrophy/adult type IV
Congenital Muscular Dystrophy
Emery-Dreifuss Muscular Dystrophy/Limb Girdle type
Muscular Dystrophy, Oculogastrointestinal type
Myopathy, Myotubular/Centronuclear
Welander syndrome (See Kugelberg Welander)