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LPL deficiency is a rare inherited disease that is characterized by severe hypertriglyceridemia, chylomicronemia, and the risk of recurrent pancreatitis, among other potential complications [8]

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After one week of levocarnitine therapy (3 doses), all patients had trough concentrations between 54 and 180 mol/L (normal 40 to 50 mol/L) and concentrations remained relatively stable or increased over the course of the study