a good long life
People with Angelman Syndrome often live the average life expectancy of their gender.
Recent advances in Marfan syndrome treatment have prolonged the life expectancy of patients considerably. Changes in how the syndrome is treated, including medication, surgical interventions, and monitoring for complications of the syndrome (eg, aneurysms), are all responsible for the increase in life expectancy. The prolongation in life expectancy can be seen by taking a look at statistics from 1972, in which the life expectancy was 32 years, and from 1996, where patients with Marfan syndrome had a life expectancy of 61 years.
people with ushers syndrome will have a normal life expectancy
If a person is severely affected by Hunter's syndrome, life expectancy is about 10 to 20 years. However, some people with the disorder life an almost normal life span.
Normal
63 years
around6years
Robinow syndrome is accompanied by heart problems that can shorten the life expectancy. if the heart problems are not severe, they can live between 13 to 20 years.
There's no shortening of life expectancy. The condition is manageable throughout the sufferers life.
rarely more than 30
With proper treatment (medications, regular checks of the aorta, preventative surgery), a person with Marfan syndrome has an average life expectancy into their mid 70s. If a person does not know they have the diagnosis or does not do proper care, the life expectancy can be the 40s. This is why proper diagnosis is key!
The life expectancy for girls with Rett Syndrome is about 44 to 48 years old. The syndrome causes physical and mental developmental problems.