Overcoming Obstacles: Expert Perspectives on the Diagnosis and Management of Familial Chylomicronemia Syndrome
Familial chylomicronemia syndrome (FCS) is an autosomal recessive disorder that affects approximately 3,000 – 5,000 individuals worldwide. Though quite rare, this disorder, characterized by elevated chylomicron levels and severe hypertriglyceridemia, presents a significant challenge both for the affected patients, as …