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Bookmark or Share- Angelman Syndrome - Symptoms, Causes, Treatment | NORDAngelman syndrome is a rare genetic and neurological disorder characterized by severe developmental delay and learning disabilities; absence or near absence of speech; inability to coordinate voluntary movements (ataxia); tremulousness with jerky movements of the arms and legs and a distinct behavioral pattern characterized by a happy dispositio...
- Angelman syndrome - WikipediaAngelman syndrome or Angelman's 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. [6]
- 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 - 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.
- Angelman syndrome: MedlinePlus GeneticsAngelman 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).
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