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Send a picture of your loved one with AS to photos@angelman.org to be included in the gallery. Include their name, date of birth and genotype.
Mar 8, 2024 · Angelman 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 (AS) is a genetic disorder that mainly affects the nervous system. 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.
Apr 7, 2022 · Angelman syndrome is a rare, complex neurodevelopmental condition that primarily affects your nervous system. It’s caused by issues with a specific gene called UBE3A. Your nervous system is your body’s command center.
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Angelman syndrome (AS) is a rare neuro-genetic disorder that occurs in one in 15,000 live births or 500,000 people worldwide. It is caused by a loss of function of the UBE3A gene in the 15th chromosome derived from the mother.
Nov 28, 2023 · 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. Features that help define the disorder include: Often, there are also gastrointestinal, orthopedic, and eye problems.
