Angelman syndrome

Angelman syndrome is a rare genetic disorder that affects the nervous system and causes severe developmental delays, speech impairments, and movement issues. It is often characterized by happy demeanor, frequent laughter, and a characteristic gait. The condition is usually caused by a deletion or mutation of the UBE3A gene on chromosome 15, which is crucial for brain function. Individuals with Angelman syndrome typically experience intellectual disabilities and may have seizures. While there is no cure, therapies and interventions, including physical and speech therapy, can help improve their quality of life and skills.