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People with Angelman syndrome tend to live close to a typical life span. But the condition can't be cured. Treatment focuses on managing medical, sleep and developmental issues.
How does Angelman syndrome affect life expectancy? Angelman syndrome is a rare disease, making it difficult to predict lifespan. However, current data suggests that the lifespan of Angelman syndrome patients is the same as someone without the disease.
What is the life expectancy of someone with Angelman syndrome? The life expectancy of people with Angelman syndrome appears to be nearly normal.
People with Angelman syndrome appear to have a reduced but near-normal life expectancy, dying on average 10 to 15 years earlier than the general population. [ 42 ] Epidemiology
The life expectancy of people with Angelman syndrome is normal. Angelman syndrome itself does not cause death. However, there can be severe complications due to some of the symptoms of the syndrome, such as seizures and aspiration pneumonia.
Angelman syndrome is a lifelong condition. People with the condition are usually unable to live independently and need support and care throughout their lives. It is estimated that the condition occurs in one out of every 12,000 to 20,000 people. It equally affects males and females.
While there is no cure for Angelman syndrome, anticonvulsant drugs, physical therapy, occupational therapy, and speech and language therapy can significantly improve the quality of life. Those affected can live normal lifespans but will invariably require lifelong care.