What is Angelman syndrome?
Angelman syndrome is a rare genetic disorder caused by a mutation in the UBE3A gene on chromosome 15. Typical symptoms include severe developmental delay, lack of or severely limited speech, motor problems and often epilepsy.
Many children with Angelman have a strikingly cheerful mood, smile or laugh frequently and appear very lively. They also experience sleep disturbances, balance problems and sometimes swallowing difficulties.
Those affected need support in many areas of life - be it communication, mobility, care or cognitive support.
Aids that are frequently used for Angelman syndrome:
Aids and support for everyday life
As people with Angelman syndrome are dependent on help for the rest of their lives, targeted aids support safety and communication:
- Augmentative and Alternative Communication (AAC): as spoken language is missing, the early introduction of AAC systems is crucial. Eye controls, iPads with communication apps (e.g. Proloquo2Go) or robust buttons enable the child to communicate their wishes and needs.
- Safety during sleep: due to pronounced sleep disturbances and the risk of epilepsy, specialized safety beds (e.g. with high, padded bars or mesh systems) are important to prevent night-time bed abandonment and injuries.
- Mobility aids: If gait is unsteady, specialized walkers or tricycles help to strengthen the muscles and explore the surroundings safely. Rehab buggies or wheelchairs are often necessary for longer distances.
- Safety in everyday life: As many children are very impulsive, safety helmets offer important safety in the event of falls or seizures. GPS trackers can also be useful for families if the child has a strong urge to move.
- Sensory integration: Heavy products such as weighted blankets or vests can help to dampen motor restlessness and help the child to become more aware of their body.
Learn more
You can find more helpful information about Angelman here:
angelman.de