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Differential Diagnosis For Weakness: Metabolic, Storage Disorders

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List of current finding(s):

Metabolic, Storage Disorders: next: Biochemical Causes
Diabetes mellitus, poorly controlled
Diabetic ketoacidosis/coma
Diabetes mellitus
Diabetic autonomic neuropathy syndrome
Diabetes mellitus/juvenile (Type I)
Diabetic amyotrophy syndrome
Diabetic peripheral neuropathy
Metabolic disorders
Porphyria, acute intermittent
Fanconi's Hereditary Renal Disease
Hemochromatosis
Cytochrome C Oxidase Deficiency/COX Complex Defect
French-Canadian type COX mitochondrial defect
Pyruvate Dehydrogenase Complex Deficiency/PDCD
Infantile mitochondrial myopathy/Cox defect
Acyl-CoA Dehydrogenase/short chain def
Lysinemia
Alpha-NAGA deficency (Schindler)
Carnitine deficiency syndrome
Fucosidosis (Anderson-Fabry)
Glutaric aciduria/type II
Glycogen storage diseases
Glycogen storage muscle disease/Pompe
McArdle's syndrome
Niemann-Pick disease
Barth Syndrome/3 MethylGlutoconic aciduria/MGA II
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