Tag: Familial chylomicronemia syndrome

Affecting approximately 1 in 1,000,000 people, lipoprotein lipase (LPL) deficiency is a rare genetic disorder that severely disrupts normal fat metabolism. The characteristic LPL deficiency lipid profile is marked by extremely high triglyceride levels and the accumulation of chylomicrons, leading to a milky appearance of the blood.

Familial chylomicronemia syndrome (FCS) is a rare genetic disorder affecting approximately one to two individuals per million, causing extremely high triglyceride levels. For those affected, a lifelong, highly restrictive very-low-fat regimen is the primary treatment, making understanding what is the diet for FCS critical for managing symptoms and preventing complications like acute pancreatitis.

Familial Chylomicronemia Syndrome (FCS), a rare genetic disorder affecting as few as one in a million people, is a severe disease where you can't have fat. It results from the body's inability to break down triglycerides from dietary fat, leading to extremely high lipid levels in the blood. This metabolic condition requires strict lifelong dietary management to prevent life-threatening complications, such as pancreatitis.