Angelman syndrome
Some of the symptoms of Angelman syndrome can be difficult to manage, and you'relikely to need help from a wide range of different healthcare professionals.
Your child may benefit from some of the following treatments and aids:
Following these studies, scientists believe it may be possible to restore UBE3A function in the brains of people with Angelman syndrome at somestage in the future.
There are also clinical trials looking at treatment for some of the symptoms associated with Angelman syndrome, such as treatments for seizures.
With age, people with Angelman syndrome become less hyperactive and the sleeping problems tend to improve. Most people with the syndrome will have intellectual disability and limited speech throughout their life.
In later childhood, the seizures usually improve, although they may return in adulthood. In adults, some mobility may be lost and joints may stiffen up. People with Angelman syndromeusuallyhave good general health, are often able to improve their communication and acquire new skills throughout their lives.
Read about Angelman syndrome, a genetic disorder that affects the nervous system and causes severe physical and intellectual disability
The typical characteristics of Angelman syndrome aren't usually apparent at birth. A child withAngelman syndrome will begin to show signs of delayed development at around 6-12 months, such as being u
In most cases of Angelman syndrome, the child's parents don't have the conditionand the genetic difference responsible for the syndrome occurs by chance around the timeof conception. The typical char
Angelman syndrome may be suspected if a child's development is delayed and they have the syndrome's distinctive characteristics (see above). A blood sample can be takento confirm the diagnosis. Anumb
Some of the symptoms of Angelman syndrome can be difficult to manage, and you'relikely to need help from a wide range of different healthcare professionals. Your child may benefit from some of the fo
The Angelman Syndrome Support Education and Research Trust (ASSERT) is a UK based charity providing information and support for parents and carers of people with the syndrome. As well as visiting th