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1:17
YouTube
The Purple Gene Clinic
Angelman Syndrome Explained | UBE3A Gene
Angelman Syndrome is a rare neurogenetic disorder caused by loss of function of the UBE3A gene on the maternal chromosome. It leads to developmental delays, speech impairment, seizures, and movement difficulties. 🧠 Key Features of Angelman Syndrome: • Severe speech delay or no speech • Seizures and abnormal EEG • Frequent laughter ...
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