Familial Hypertrophic Cardiomyopathy and Sustainable Healthcare: Genetic Insights, Clinical Implications, and Future Therapeutic Strategies for Global Health

Familial Hypertrophic Cardiomyopathy and Sustainable Healthcare: Genetic Insights, Clinical Implications, and Future Therapeutic Strategies for Global Health

Authors

  • Dr. Prasad Mettikolla

Abstract

Familial Hypertrophic Cardiomyopathy (FHC) is a genetic disorder characterized by abnormal thickening of the heart muscle, often leading to serious cardiovascular complications, including heart failure and sudden cardiac death. This review provides a comprehensive overview of the molecular mechanisms underlying FHC, emphasizing the role of sarcomeric protein mutations and their impact on cardiac function. Advances in genetic screening, particularly in identifying at-risk individuals, are discussed alongside the evolving landscape of clinical diagnostics, including imaging techniques and biomarker assessments. We also examine the latest therapeutic approaches, ranging from pharmacological treatments to innovative interventions like gene therapy and myectomy. The implications for personalized medicine, risk stratification, and long-term management are explored, aiming to improve patient outcomes and quality of life. Future research directions and challenges in bridging the gap between genotype and phenotype are highlighted

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Published

2023-09-30

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How to Cite

Familial Hypertrophic Cardiomyopathy and Sustainable Healthcare: Genetic Insights, Clinical Implications, and Future Therapeutic Strategies for Global Health. (2023). International Journal of Sustainable Development Through AI, ML and IoT, 2(2), 1-25. https://ijsdai.com/index.php/IJSDAI/article/view/69

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