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Differential Diagnosis For Muscle weakness: Metabolic, Storage Disorders

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List of current finding(s):

Metabolic, Storage Disorders: next: Biochemical Causes
Diabetic amyotrophy syndrome
Diabetic peripheral neuropathy
Metabolic disorders
Fanconi's Hereditary Renal Disease
Tay-Sachs disease
Xanthinuria
Cytochrome C Oxidase Deficiency/COX Complex Defect
French-Canadian type COX mitochondrial defect
Infantile mitochondrial myopathy/Cox defect
Acyl-CoA Dehydrogenase/short chain def
Carnitine deficiency syndrome
Fucosidosis (Anderson-Fabry)
Glycogen storage diseases
Glycogen storage muscle disease/Pompe
McArdle's syndrome
Neutral lipid storage disease
Niemann-Pick disease
Sandhoff disease
Von Gierke's disease/glycogenosis I
Barth Syndrome/3 MethylGlutoconic aciduria/MGA II
Lysosome Storage Disease
Myoadenylate deaminase deficiency
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