Crafted for healthcare professionals and individuals alike, 'Familial Hypercholesterolemia: Insights into Diagnosis, Treatment, and Personalized Care' offers a comprehensive exploration of this inherited lipid disorder. Delving into the intricate interplay of genetics, lipoprotein metabolism, and cardiovascular health, this treatise provides valuable insights into the diagnosis, management, and personalized care of familial hypercholesterolemia (FH). From elucidating the genetic basis and inheritance patterns to unraveling the pathophysiological mechanisms and cardiovascular manifestations, each chapter offers a nuanced understanding of FH. With a focus on evidence-based approaches, the treatise navigates through clinical evaluation, laboratory investigations, imaging studies, and challenges in diagnosis, offering practical guidance for healthcare providers. Moreover, it delves into lifestyle modifications, pharmacological interventions, and emerging therapies, emphasizing personalized strategies to optimize treatment outcomes and improve quality of life for individuals living with FH. 'Familial Hypercholesterolemia: Insights into Diagnosis, Treatment, and Personalized Care' serves as a valuable resource for clinicians, researchers, and individuals affected by FH, empowering them with knowledge to navigate this complex condition effectively.