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Differential Diagnosis For Weakness: Hereditary, Familial, Genetic Disorders

List of current finding(s):

Hereditary, Familial, Genetic Disorders: next: Degenerative-Age Related Causes: Periodic paralysis, hypokalemic; Thyrotoxic periodic paralysis; Duchenne's Muscular Dystrophy/Pseudohypertrophic; Erb's Muscular Dystrophy/Limb Girdle MD; Gardner syndrome; Infantile neuroaxonal dystrophy; Muscular dystrophy; Muscular dystrophy, limb girdle type; Muscular dystrophy, progressive; Neuropathy, hypertrophic interstitial; Paraplegia, spastic hereditary; Peroneal muscular atrophy(Charcot Mar.); Spinal muscle atrophy; Spinal muscle atrophy, infantile; Juberg Marsidi Genetic syndrome (unco); Juvenile spinal muscle atrophy (Kugelberg-Welander); Marinesco Sjogren syndrome; Mitochondrial myopathy/MERRF; Periodic paralysis, familial; Gittleman's syndrome; Pseudohypoparathyroidism; Dominant SCA/Spinal Cerebellar ataxias; Bartter's syndrome; Dysautonomia, familial; Encephalomyelopathy/necro/subact/Leigh; Facioscapulohumeral muscular dystrophy; Friedreich's Ataxia; Kearns-Sayre Ophthalmoplegic Syndrome; Muscular atrophy, infantile, spinal; Myotonia atrophica (Steinert's disease); Nemaline myopathy; Nephritis, familial interstitial; Schwartz-Jampel syndrome; Spinal muscle atrophy/adult type IV; Familial Vitamin D dependent Rickets; Myopathy, Desmin Storage type/Sarcoplasmin bodies; Myopathy, Myotubular/Centronuclear; Welander syndrome (See Kugelberg Welander)

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