Familial chylomicronemia syndrome: Revision history

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31 May 2024

  • curprev 20:0920:09, 31 May 2024‎ Ai talk contribs‎ 5,525 bytes +5,525‎ 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..."
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