Given the particulars of Angelman syndrome, it is certainly understandable for a person to want to learn as much as they possibly can about this disease. One of the most important questions a person is likely going to ask themselves concerns the life expectancy of those who have an Angelman syndrome diagnosis.
This is an excellent and understandable question to ask, but it cannot be answered without a proper foundation in understanding what this disease is all about.
Angelman Syndrome and Life Expectancy
Life expectancy is one facet to a strong understanding of Angelman Syndrome. There are other things a person who wants to learn more about the disease is going to want to understand:
1. Angelman Syndrome is a genetic disorder.
2. The primary features of the condition involve a substantial speech impairment, developmental delays, intellectual disabilities, and difficulties concerning movement and balance (this is known as ataxia).
3. The syndrome is named after Harry Angelman. He defined the condition in the 1960’s.
4. Angelman syndrome is capable of impacting one in anywhere between twelve and twenty thousand people.
5. Children who suffer from Angelman syndrome can also experience microcephaly and epilepsy.
6. With children who suffer from Angelman syndrome, the developmental delay component can be noticed between the ages of six months to twelve months.
7. The seizure aspect of the disease can begin to appear in children who are between the ages of two and three.
8. Distinct, “abrasive” facial features are found in many adults who suffer from Angelman syndrome.
9. Since there is no specific treatment course for Angelman syndrome, handling the condition usually involves combining several established forms of treatment. These can include physical therapy, occupational therapy, and speech therapy.
10. In most cases, the range of treatments available to someone who suffers from Angelman syndrome can make it possible for that person to achieve their maximum potential in life.
Although there are many difficult, unfortunate aspects to Angelman syndrome, the overall prognosis offers certain measures of comfort. This condition does not typically impact how long a person is going to live. It is entirely possible for a person to live a long, physically healthy life with Angelman syndrome. It is not possible for this specific condition to get worse for someone as they get older.
Early detection is crucial with Angelman syndrome. This ensures that treatment can begin as soon as possible. Treatment and individualized interventions can give the person in question the highest quality of life that will be available to them.
