Familial Hypercholesterolemia (FH): A Genetic Disorder Affecting Millions in Europe

Familial Hypercholesterolemia (FH) is a genetic disorder that affects hundreds of thousands of people in Germany alone and millions across Europe. Characterized by extremely high LDL cholesterol concentrations, FH significantly increases the risk of premature cardiovascular disease. Despite its prevalence, less than 1% of affected individuals are diagnosed, leaving a substantial number untreated. Moreover, only a small minority of diagnosed and treated patients achieve optimal LDL cholesterol levels.

Early diagnosis and effective treatment are crucial in managing FH. This book provides a comprehensive overview of the pathophysiology, diagnosis, and established and novel therapeutic approaches for FH. The user-friendly format, featuring tables, graphs, and “Q&A” sections, answers the most common questions from medical practice with simple and precise responses.

A Valuable Resource for Healthcare Professionals

This book is an invaluable resource for general practitioners, internists, and cardiologists seeking to enhance their understanding of FH and provide optimal care for their patients. With its accessible language and clear structure, it is an essential tool for healthcare professionals dedicated to improving patient outcomes.

Book Details:

• Language: German
• Publisher: UNI-MED Verlag AG
• Edition: 2nd edition
• Publication Date: September 23, 2015
• ASIN: B09FS186CZ