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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.
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.
Apr 7, 2022 · Angelman 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.
Jul 19, 2024 · 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: Developmental delay. Intellectual disability. Severe speech impairment. Problems with movement and balance (ataxia)
Angelman syndrome is a complex genetic disorder that primarily affects the nervous system. Characteristic features of this condition include delayed development, intellectual disability, severe speech impairment, and problems with movement and balance (ataxia).
Feb 14, 2018 · Learn about Angelman Syndrome, including symptoms, causes, and treatments. If you or a loved one is affected by this condition, visit NORD to find resources.
