[13] The following hereditary disorders of the muscle energy supply may cause recurrent and usually exertional rhabdomyolysis: [10] [13] [17] Glycolysis and glycogenolysis defects: McArdle's disease, phosphofructokinase deficiency, glycogen storage diseases VIII, IX, X and XI Lipid metabolism defects: carnitine palmitoyltransferase I and II deficiency, deficiency of subtypes of acyl CoA dehydrogenase (LCAD, SCAD, MCAD, VLCAD, 3-hydroxyacyl-coenzyme A dehydrogenase deficiency), thiolase deficiency Mitochondrial myopathies: deficiency of succinate dehydrogenase, cytochrome c oxidase and coenzyme Q10 Others: glucose-6-phosphate dehydrogenase deficiency, myoadenylate deaminase deficiency and muscular dystrophies Mechanism [edit] Damage to skeletal muscle may take various forms
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Liraglutide uses Liraglutide can be used to both manage weight and improve blood sugar
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Fiber can slow the absorption of some oral medications
While this is not a known direct effect of GLP-1 therapy, it still needs attention