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Differential Diagnosis For Weakness: Hereditary, Familial, Genetic Disorders

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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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