Tag: rare genetic disorder


Angelman Syndrome: Symptoms, Causes & Support

Introduction and Definition Angelman Syndrome (AS) is a complex, neurodevelopmental genetic disorder that profoundly impacts the nervous system, leading to characteristic symptoms such as severe intellectual disability, developmental delay, ataxia (problems with balance and movement), and a unique behavioral phenotype often described as excessively cheerful or happy. First identified clinically by Dr. Harry Angelman in […]

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