Explore the world of Familial Hypercholesterolemia (FH) in this comprehensive webinar. Delve into clinical signs and symptoms, diagnostic criteria, genetics, and genetic testing for this inherited condition characterized by high cholesterol levels. Learn about treatment options, available resources, and relevant events. Gain insights into the study populations, countries affected, and the differences between homozygous and heterozygous FH. Understand the cholesterol distribution, AHA scientific statements, and the pathophysiology of FH. Discover the genes associated with FH, LDL mutations, and genetic testing guidelines. Examine the clinical and mutation overlap, public health implications, and the importance of cascade testing. Review screening recommendations for children and adults, cost-effective tools, and treatment options, including LDL cholesterol burden management and non-invasive imaging. Explore consultation with lipid specialists, medications like Kynamro and PCSK9 inhibitors, and additional resources to enhance your understanding of this genetic disorder. Read more