Fragile X Syndrome is a genetic condition that causes developmental delays, intellectual disabilities, and behavioral challenges, affecting both males and females. This article is a comprehensive guide that explains the condition in detail, offering valuable information for patients, families, and caregivers. It begins with an introduction to the disorder, describing its impact on individuals and families. The article provides an overview of the genetic causes of Fragile X Syndrome, particularly the role of the FMR1 gene, and explains how the condition is inherited. It explores the symptoms and their variability, ranging from cognitive and behavioral challenges to physical features. The diagnostic process, including genetic testing and the importance of early detection, is thoroughly addressed. The article also outlines current treatment and management strategies, highlighting therapies, medications, and emerging research aimed at improving quality of life. It discusses the prognosis and offers practical advice for living with Fragile X Syndrome, emphasizing the importance of early interventions and supportive environments. The article is structured to provide a logical flow of information, from understanding the condition to managing its challenges. Written in clear, straightforward language, it ensures that the content is accessible and easy to understand for all readers seeking to learn about Fragile X Syndrome.