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Primary carnitine deficiency (PCD) is an autosomal recessive disorder of mitochondrial -oxidation resulting from defective carnitine transport and is one of the rare treatable etiologies of metabolic cardiomyopathies
Routine liver enzyme monitoring is not required for otherwise healthy patients taking GLP-1 medications
That schedule is baked into the drugs design and pharmacokinetics
Cozzolino M, Seli E
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