Early diagnosis and intensive intervention offer the best prognosis for individuals with fragile X syndrome. Adults with fragile X syndrome may benefit from vocational training and may need to live in a supervised setting. Life span is typically normal
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.
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.
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!
a good long life
people with ushers syndrome will have a normal life expectancy
life expectancy is shortened but recent research demonstrate that mortality rate is less than reported in the past and that mortality rate correlates with the size of the deletion
The average life expectancy of a person with Down syndrome is 50 in 2013. However, many individuals with Down syndrome live into their 60s and 70s. Some do well on their own and others need help.
63 years
Normal
Yes. Along with the Down they often have other physical problems such as enlarged hearts and immune problems, so they often die of something other than Down syndrome directly. Many die in their teen or early adult years.
Life expectancy can vary for individuals with Robinow syndrome depending on the severity of their symptoms and associated complications. In general, most individuals with Robinow syndrome have a normal lifespan, but some may experience health issues that can affect their life expectancy. It is important for individuals with Robinow syndrome to receive regular medical monitoring and appropriate care to manage their condition.
The life expectancy of someone with Job syndrome (Hyper-IgE syndrome) varies based on individual health and medical management. With proper treatment, such as antibiotics for infections and managing associated complications, many individuals with Job syndrome can live into adulthood. However, there can be a higher risk of certain complications that may affect life expectancy.