This episode provides a comprehensive overview of Angelman syndrome, a rare genetic disorder. It covers the condition's history, genetic causes, characteristic symptoms, and diagnostic processes. Listeners will gain insights into the challenges faced by individuals with Angelman syndrome and their families, as well as learn about current research and future treatment possibilities. This informative exploration is suitable for families, caregivers, medical professionals, and anyone interested in rare genetic conditions.
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Aug 13 202425 mins