Familial Hypercholesterolemia: Improving Detection to Accelerate Treatment
Familial hypercholesterolemia (FH) is the most common autosomal-dominant genetic disorder, affecting approximately 30 million patients worldwide and characterized by lifelong elevations in low-density lipoprotein cholesterol (LDL-C). Review the newest expert analysis, Homozygous Familial Hypercholesterolemia: Diagnosis and Emerging Therapies, and learn the indicators to look out for to make the diagnosis of familial hypercholesterolemia with the Could it be FH? Recognizing Familial Hypercholesterolemia infographic. Improve detection and diagnosis of FH and increase familiarity with the new treatment options available to the cardiovascular community with the Familial Hypercholesterolemia: Improving Detection to Accelerate Treatment online course.