Labels:text | screenshot | black | black and white OCR: onally a genetic The chylomicronaemia syndrome occas CII. Much occurs when LPL is inactive as a result o defect in the enzyme or its cofactor, apo if the more commonly, it is due to saturation result of thecapacity of LPL to remove triglyceride, a coexistence of a genetic form of plasma hypertriglyceridaemia with a disorder of e due to triglyceride metabolism. The latter may 8 one or more diseases, or to drugs (Fig. 6.
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