This series on Angelman syndrome explores the condition from its genetic origins to daily life challenges and future research. In Part 1, we delve into the syndrome's symptoms, causes, and diagnosis. Part 2 focuses on living with Angelman syndrome, covering early development, therapies, and the role of support networks. The series concludes with Part 3, highlighting current research, potential breakthroughs, and the importance of advocacy for those affected by this rare genetic disorder.