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Differential Diagnosis For Muscle weakness: Hereditary, Familial, Genetic Disorders


List of current finding(s):

Hereditary, Familial, Genetic Disorders: next: Degenerative-Age Related Causes
Thyrotoxic periodic paralysis
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
Juberg Marsidi Genetic syndrome (unco)
Juvenile spinal muscle atrophy (Kugelberg-Welander)
Kennedy Muscular atrophy disease
Marinesco Sjogren syndrome
Mitochondrial myopathy/MERRF
Gittleman's syndrome
MELAS Encephalopathy
Bartter's syndrome
Central core disease
Distal muscular dystrophy (Gowers)
Facioscapulohumeral muscular dystrophy
Kearns-Sayre Ophthalmoplegic Syndrome
Muscular atrophy, infantile, spinal
Nemaline myopathy
Nephritis, familial interstitial
Schwartz-Jampel syndrome
Spinal muscle atrophy/adult type IV
Congenital Muscular Dystrophy
Emery-Dreifuss Muscular Dystrophy/Limb Girdle type
Familial Vitamin D dependent Rickets
Myopathy, Desmin Storage type/Sarcoplasmin bodies
Myopathy, Myotubular/Centronuclear
Welander syndrome (See Kugelberg Welander)