What is Angelman Syndrome?

Angelman syndrome is a rare genetic condition affecting the nervous system, caused by a missing or non-functioning copy of a specific gene inherited from the mother. It typically becomes apparent in the first year or two of life, as developmental delays become noticeable.

Children with Angelman syndrome often have delayed development, difficulty with speech, problems with balance and movement, and a happy, excitable demeanour with frequent smiling and laughter. Many also experience seizures. While there's no cure, early intervention with therapies can make a significant difference to a child's development and quality of life.