D The Fellowship of Postgraduate Medicine, Lipoprotein lipase deficiency due to long-term heparinization presenting as severe hypertriglyceridaemia. The enzyme lipoprotein lipase (LPL) is a glycoprotein located on the luminal surface of capillary PDF · Lipoprotein Deficiency Syndromes pp | Cite as. Familial lipoprotein lipase deficiency is an inherited condition that disrupts the normal breakdown of fats in the body, resulting in an increase of. The National Organization for Rare Disorders. NORD Guides for Physicians. The Physician's Guide to. Lipoprotein Lipase. Deficiency (LPLD). LPLD is a rare condition that affects about one in a million of the population. People who have the condition are unable to produce enough lipoprotein lipase, the. The enzyme lipoprotein lipase (LPL) is a glycoprotein located on the luminal surface of capillary endothelial cells (see reviews: ). It is bound to a. Lipoprotein lipase deficiency (LPLD) is an autosomal recessive inherited disorder caused by loss-of-function mutations in genes involved in the. Lipoprotein lipase deficiency and CETP in streptozotocin-treated apoB- expressing mice. Yuko Kako, Maureen Massé, Li-Shin Huang, Alan R. Tall, and Ira J. Lipoprotein Lipase Deficiency in an Infant. Article (PDF Available) in Indian pediatrics 48(10) · October with Reads. Source.