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Differential Diagnosis For Family history/Muscle disease/Muscular dystrophy


List of current finding(s):

Metabolic, Storage Disorders
Glycogen storage muscle disease/Pompe
McArdle's syndrome
Barth Syndrome/3 MethylGlutoconic aciduria/MGA II
Congenital, Developmental Disorders
Slow Channel Myasthenic Syndrome
Hereditary, Familial, Genetic Disorders
Periodic paralysis, hypokalemic
Duchenne's Muscular Dystrophy/Pseudohypertrophic
Erb's Muscular Dystrophy/Limb Girdle MD
Peroneal muscular atrophy(Charcot Mar.)
Juvenile spinal muscle atrophy (Kugelberg-Welander)
Myotonia atrophica (Steinert's disease)
Myotonia congenita (Thomsens d.)
Oculopharyngeal muscular dystrophy
Congenital Muscular Dystrophy
Myopathy, Myotubular/Centronuclear
Welander syndrome (See Kugelberg Welander)
Congenital progressive muscular dystrophy, Dystrophic muscle disease or syndrome, Dystrophic Muscle Diseases and Syndromes, Dystrophies Muscular, Dystrophy (Muscular), Dystrophy Muscular, dystrophy muscular congenital (hereditary) (progressive), dystrophy muscular hereditary (progressive), dystrophy muscular progressive (hereditary), Family history, Hered.progres.musc.dystr., Heredit.progres.musc.dystrophy, Hereditary progressive muscular dystrophy, Hereditary progressive muscular dystrophy (disorder), MD Muscular dystrophy, Muscular Dystrophies, Muscular Dystrophy, Muscular dystrophy (disorder), muscular dystrophy congenital (hereditary) (progressive), muscular dystrophy hereditary (progressive), muscular dystrophy progressive (hereditary), Muscular dystrophy syndrome, Myodystrophica, Myodystrophicas, Myodystrophies, Myodystrophy, PMD Progressive muscul dystr, PMD Progressive muscular dystrophy, Progressive muscular dystrophy, Progressive muscular dystrophy hereditary
External Links Related to Family history/Muscle disease/Muscular dystrophy
PubMed (National Library of Medicine)
NGC (National Guideline Clearinghouse)
Medscape (eMedicine)
Harrison's Online (accessmedicine)
NEJM (The New England Journal of Medicine)