Angelman Syndrome: A Rare and Complex Neurodevelopmental Condition

What is Angelman Syndrome?

Angelman syndrome (AS) is a rare genetic disorder characterized by significant developmental and neurological challenges. It affects about one in 15,000 people worldwide.

Symptoms of Angelman Syndrome

The symptoms of AS typically appear in early childhood and may include:

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• Developmental delays
• Intellectual disability
• Speech and language difficulties
• Motor coordination issues
• Unusual facial features, such as a wide mouth and a prominent chin
• Seizures
• Sleep disturbances