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  • Title: Familial chylomicronemia in a nine months old infant.
    Author: Lone SW, Imdad A, Billoo AG.
    Journal: J Coll Physicians Surg Pak; 2008 Oct; 18(10):655-6. PubMed ID: 18940129.
    Abstract:
    Familial chylomicronemia syndrome is a rare disorder of lipoprotein metabolism due to familial lipoprotein lipase or apolipoprotein C-II deficiency or the presence of inhibitors to lipoprotein lipase. It manifests as eruptive xanthomas, acute pancreatitis, and lipaemic plasma due to marked elevation of triglyceride and chylomicrons levels. We report a rare case of familial chylomicronemia in a 9-month-old infant, who was diagnosed after his plasma was incidentally found to be milky. Lipid profile showed familial chylomicronemia (Type 1 Hyperlipidemia). The infant was started on a low fat diet and advised a regular follow-up.
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