a side-to-side curvature of the spine (scoliosis).skin, hair and eyes that are paler than other family members.Other possible features of the syndrome include: Children with Angelman syndrome may also start to have seizures or fits around this age. trouble sleeping and needing less sleep than other childrenīy around 2 years of age, a small head which is flat at the back (microbrachycephaly) may be noticeable in some children with Angelman syndrome.being easily excitable, often flapping the hands.frequent laughter and smiling, often with little stimulus.Several distinctive behaviours are associated with Angelman syndrome. These include: Their arms may tremble or make jerky movements, and their legs may be stiff. They may have difficulty walking because of issues with balance and co-ordination (ataxia). The movement of a child with Angelman syndrome will also be affected. However, most children with Angelman syndrome will be able to communicate using gestures, signs or other systems. Later, they may not speak at all or may only be able to say a few words.
Characteristics of Angelman syndromeĪ 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. Angelman syndrome is a genetic condition that affects the nervous system and causes severe physical and learning disabilities.Ī person with Angelman syndrome will have a near-normal life expectancy, but they will need support throughout their life.
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