30+ Angelman Syndrome Background. Due to the common characteristics, misdiagnosis occurs. Angelman syndrome is a complex genetic disorder that primarily affects the nervous system.
Rush University Medical Center Launches Angelman Syndrome Clinic from www.rush.edu
Clinical, cytogenetic, and molecular diagnosis of angelman syndrome. Characteristic features of this condition include delayed development, intellectual disability. Angelman syndrome is caused by a genetic mutation on chromosome 15.
Angelman syndrome is a rare genetic condition that primarily affects the central nervous system, causing physical and intellectual disability.
Angelman syndrome is a rare genetic condition that primarily affects the central nervous system, causing physical and intellectual disability. Patients with angelman syndrome still develop sexually, which raises many important concerns for them and their caregivers as they age. It causes delayed development, problems with speech and balance, intellectual disability, and sometimes, seizures. Angelman syndrome is a genetic disorder that affects the nervous system and causes severe physical and intellectual disability.
