Angelman syndrome is a rare neurodevelopmental disorder caused by the loss of a gene called UBE3A on the mother’s copy of chromosome 15. It affects people of all races and ethnicities and often appears in infancy through feeding difficulties, delayed motor skills, and limited speech development. Individuals with Angelman syndrome experience complex challenges, including seizures and sleep disruptions, yet many also show a deep connection with those around them - smiling, laughing and maintaining
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Angelman syndrome is a rare disorder that affects chromosome 15, resulting in intellectual and developmental delay. Common signs and symptoms usually appear in early childhood but despite these symptoms, people with Angelman syndrome have an overall happy and excitable demeanor. #InternationalAngelmanDay #angelmanday2024 | Angelman Syndrome Foundation
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