Introduction: Angelman syndrome


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Angelman syndrome: Prader-Willi syndrome and Angelman syndrome are two rare chromosome disorders, with very different symptoms, but caused by the same area of DNA. They are important to genetic research because they are caused by imprinting.

Angelman syndrome: Angelman syndrome is a neurological disorder characterized by severe congenital mental retardation, unusual facial appearance, and muscular abnormalities. 1

Researching symptoms of Angelman syndrome: Further information about the symptoms of Angelman syndrome is available including a list of symptoms of Angelman syndrome, symptom statistics for Angelman syndrome, or alternatively return to research other symptoms in the symptom center.

Treatments for Angelman syndrome: Various information is available about treatments available for Angelman syndrome, symptom statistics for Angelman syndrome, or research treatments for other diseases.

Statistics and Angelman syndrome: Various sources and calculations are available in statistics about Angelman syndrome, symptom statistics for Angelman syndrome, prevalence and incidence statistics for Angelman syndrome, and you can also research other medical statistics in our statistics center.

         Contents for Angelman syndrome:

Footnotes:
1. excerpt from NINDS Angelman Syndrome Information Page: NINDS

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