Abstract
Sepsis, a life-threatening condition resulting from the body's extreme response to infection, remains a global health challenge with high morbidity and mortality rates. The primary aim of this article is to unravel the intricate genetic factors contributing to sepsis susceptibility, severity, and patient outcomes. By understanding the genomic landscape of sepsis and its pathogenic infiltrations, this article tries to contribute to the development of novel diagnostic tools and therapeutic interventions, additionally it tries to integrate genomic data with clinical information to develop personalized approaches for sepsis management, including targeted therapies, drug development and precision medicine, and improving overall outcomes for individuals affected by Sepsis.
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