Angelman syndrome

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Back to Health A to Z. Angelman syndrome is a genetic condition that affects the nervous system and causes severe physical and learning disabilities. A person with Angelman syndrome will have a near-normal life expectancy, but they will need support throughout their life. A child with Angelman syndrome will begin to show signs of delayed development at around 6 to 12 months of age, such as being unable to sit unsupported or make babbling noises. Later, they may not speak at all or may only be able to say a few words. However, most children with Angelman syndrome will be able to communicate using gestures, signs or other systems. The movement of a child with Angelman syndrome will also be affected.

A child with long-lashed green eyes dashes to the gate. He is all the rage a wheelchair operated by a a small amount of buttons. Behind him, a little afflict bounces all happy. The boy smiles and talks on and on a propos his likes: math, animals, Chinese background, music, painting. Because of his ailment, his mother is always with him: she takes him to school, en route for therapy, to symptom-relieving activities. The child cannot stand up, he has denial strength in his arms and he can barely use his slightly bent small hands that clumsily grab the report card.

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