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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

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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Establishing a diagnosis of PHG disease caused by HSV-1 infection actually could be seen from the patients anamnesis and clinical examination, such as in the study by Turton et al which stated that the characteristics of perioral vesicles, ulcers in the oral cavity including the gingiva, inflammation of the gingival margin area and starting with prodromal symptoms are very common symptoms in PHG without conducting supporting examinations

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