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Angelman Syndrome: What Is, Causes, Symptoms, and Early Signs

What is Angelman Syndrome?

Angelman syndrome: This is a rare genetically determined disease. The essence of the condition is a disorder of the nervous system involving mental and motor impairment and facial dysmorphic changes. The disease can be confused with cerebral palsy and Autism. The first description of pediatric patients with a characteristic facial appearance was made in 1965 by British pediatrician Harry Angelman.

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