Angelman syndrome occurs where there is a genetic issue that affects children within the first 2-3 years of life and stays present throughout adulthood. First described as an issue in 1965 by Dr. Harry Angelman, children have developmental delays and neurological problems that often include seizures. There are also speech impairments in place and many kids with this syndrome may not choose to speak at all. Here are some more interesting facts about this syndrome to consider as well.
1. Early intervention is the key to a successful treatment.
Although there isn’t a cure for Angelman syndrome, there are some effective treatments that are in place to help children with this disorder. The earlier these interventions can take place, then the more effective a treatment plan is able to be. Children who have the earliest interventions tend to be the most successful with their lives as their progress is charted into adulthood.
2. It isn’t a regressive disorder.
Most people who are born with Angelman syndrome don’t experience any regression in the intelligence they are able to obtain. This means that many kids are able to eventually catch up to their peers if they are given enough time, coaching, counseling, and there are monetary resources which are available. The one place that will continue on aggressively without medical treatment with this syndrome is with the seizures.
3. There is a lot of energy present every day.
Those who have Angelman syndrome typically have a hyperactive amount of energy that is present. There is so much energy, in fact, that people with this genetic disorder can have regular bouts of insomnia because they are too energized to get to sleep. Sometimes this can cause issues with balance and movement, eventually leading to deficits in the functioning that can be difficult to overcome if they occur.
4. It is difficult to recognize Angelman syndrome in infancy.
Most of the development issues of Angelman syndrome do not make themselves known in early infants, which is unfortunately because of how critical early interventions happen to be. Sometimes children may have a prominent chin, but for the most part, they have the same facial characteristics as their family. It is distinctive, however, because the behaviors and developmental course is completely unique. Not every behavior or developmental issue needs to be present for the disorder to be diagnosed.
5. Not every child has seizures.
Those with Angelman syndrome are known for the seizures that typically happen around the 2-3 year old mark, but that isn’t necessarily an indicator of the disorder. About 20% of those who have this syndrome don’t suffer from any seizures at all. Even when seizures are present, most children are able to eventually outgrow them so that they are able to have a happy, fulfilling life.
Angelman syndrome produces a unique set of difficulties, but that doesn’t have to affect a person’s quality of life. By knowing these facts, the right levels of support can be found if Angelman Syndrome is suspected.