Fragile X Syndrome: Public Education

Abstract

Fragile X Syndrome is a genetic condition that affects both males and females, leading to developmental delays, intellectual disabilities, and behavioral challenges. This article offers a comprehensive overview of the disorder, explaining its genetic causes, symptoms, diagnosis, and management in clear and simple terms. Fragile X Syndrome results from mutations in the FMR1 gene, which disrupts the production of a protein critical for normal brain development. With information tailored to patients, families, and caregivers, this book covers the impact of Fragile X Syndrome on daily life and provides insights into available treatments, support systems, and ongoing research.