Medical EditorDr. Nicholas Bush MBBS BSc (Hons)
2 min read
Last Updated: 8 August 2024
Angelman Syndrome
Medical EditorDr. Nicholas Bush MBBS BSc (Hons)
2 min read
Last Updated: 8 August 2024
Angelman Syndrome
Angelman syndrome is a rare genetic disorder affecting the nervous system. It is caused by a deletion or mutation in the UBE3A gene on chromosome 15. Symptoms include severe developmental delays, speech impairments, frequent laughter, balance issues, and epilepsy. Diagnosis typically involves genetic testing, and there is no cure currently available for Angelman syndrome.
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