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About Angelman Syndrome

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Angelman Syndrome is a genetic condition affecting around 1 in 15,000 children. It stems from a deletion in the maternal chromosome 15, deletions in the same region of the paternal chromosome result in Prader-Willi Syndrome.

Angelman Syndrome is usually, but not always, diagnosed in toddlerhood.

Angelman Syndrome is associated with severe learning difficulties, speech impairment, short attention-span, balance and coordination problems and a very much higher than average incidence of epilepsy.

Children with Angelman Syndrome have a characteristically joyful demeanour but it should be noted that this is feature of the condition and not always an indicator of an individual's underlying mood or a feeling of well-being.

  • Angelman Syndrome Foundation
    The ASF is a US charity dedicated to providing support and information to families. Their website is an excellent source of information.
     
  • ASSERT
    UK based Angelman Syndrome support group run by volunteers with direct experience of the condition, generally parents and family members.
     
  • IASO
    The International Angelman Syndrome Organisation is an umbrella organisation of many national charities and support organisations.