About Angelman Syndrome | Recommended Links |
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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.
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