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Discussion and conclusions Carnitine palmitoyltransferase II (CPTII) deficiency is a rare autosomal recessive disorder of mitochondrial fatty acid oxidation, due to biallelic pathogenetic variants in CPT gene, whose locus is in 1p32.3 [1]

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Cardiovascular exercise helps too, but prioritize resistance training if time is limited

The specific reasons identified include intensive insulin therapy, decreased renal function, severe liver disease, alcohol ingestion, defective counter regulatory hormone release, missing meals/fasting, and gastroparesis

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