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Bookmark or Share- Angelman Syndrome: What It Is, Symptoms & Treatment - Cleveland ClinicAngelman syndrome is a rare and complex neurodevelopmental condition that causes developmental delays, intellectual disabilities, speech impairments and movement issues. It’s caused by issues with a specific gene called UBE3A that happens during fetal development.
- Angelman syndrome - WikipediaAngelman syndrome (AS) is a genetic disorder that mainly affects the nervous system. [6] Symptoms include a small head and a specific facial appearance, severe intellectual disability , developmental disability , limited to no functional speech, balance and movement problems, seizures, and sleep problems. [ 6 ]
- Angelman Syndrome - StatPearls - NCBI BookshelfAngelman syndrome (AS) is caused by a pathologic lack of expression of the UBE3A gene on the maternal chromosome in combination with physiologic genomic imprinting or silencing on the paternal chromosome in neurons.
- Angelman syndrome - Symptoms and causes - Mayo ClinicAngelman syndrome is a condition caused by a change in a gene, called a genetic change. Angelman syndrome causes delayed development, problems with speech and balance, mental disability, and, sometimes, seizures.
- Angelman Syndrome - National Institute of Neurological Disorders and StrokeWhat is Angelman syndrome? Angelman syndrome is a genetic disorder that primarily affects the nervous system. The disorder is named after Dr. Harry Angelman who first reported the syndrome in 1965.
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