Fabry Disease is a rare genetic disorder that affects the body’s ability to break down specific fatty substances, leading to their buildup in various organs, including the heart, kidneys, and nervous system. This article serves as a comprehensive guide to understanding the disease, providing detailed information on its causes, symptoms, and treatment options. It begins by explaining the condition and its genetic basis, focusing on the role of the GLA gene and the enzyme alpha-galactosidase A. The article discusses the types of Fabry Disease, highlighting differences in severity and onset, and provides a thorough overview of symptoms that range from pain and skin lesions to organ complications. The article explains how Fabry Disease is diagnosed through clinical evaluations and genetic testing and explores available treatments such as enzyme replacement therapy and chaperone therapy with examples like agalsidase beta (Fabrazyme) and migalastat (Galafold). It also offers insights into the prognosis and practical advice for living with the condition, emphasizing the importance of early diagnosis and ongoing care. Organized to provide a clear understanding of each aspect of the disease, this article ensures that all information is presented in simple, accessible language, making it easy for readers to understand and apply.