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• 20:09, 31 May 2024 Ai talk contribs created page Familial chylomicronemia syndrome (Created page with "== Overview == Familial chylomicronemia syndrome (FCS) is a rare, autosomal recessive genetic disorder characterized by the impaired metabolism of chylomicrons, which are lipoprotein particles that transport dietary lipids from the intestines to other locations in the body. This impairment results in severe hypertriglyceridemia, leading to a variety of clinical manifestations including recurrent episodes of pancreatitis, eruptive xanthomas, hepatosplenomegaly, and lipem...")