It depends on many factors, and there is a great deal of variability in the syndrome and the health problems associated with it.
This report is probably the best compilation on the subject. It is available in the Literature section of http://clsf.info.
Coffin-Lowry Syndrome: A 20-Year Follow-Up and Review of Long-Term Outcomes American Journal of Medical Genetics111:345-355 (2002)
Chairperson
Coffin-Lowry Syndrome Foundation
i think it only matters on the the person and what the person has specifically
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.
Individuals with Angelman syndrome typically have a normal life expectancy, as the condition itself is not life-threatening. However, they may face challenges in terms of cognitive and physical development, as well as require ongoing support and care throughout their lives. Regular medical monitoring and interventions can help manage associated symptoms and improve quality of life.
Life expectancy for individuals with Bardet-Biedl syndrome can vary greatly depending on the severity of their symptoms and medical management. Many individuals with this syndrome can live into adulthood with appropriate medical care and monitoring. However, complications associated with the syndrome, such as obesity-related issues and kidney problems, can impact life expectancy.
The life expectancy of someone with gout is generally the same as the general population, as long as the condition is managed properly and other health factors are taken into consideration.
A deletion or other structural modification of the terminal end of chromosome 22 in the 22q13 region, or a disease-causing (pathogenic) variation of the SHANK3 gene, causes Phelan-McDermid syndrome (PMS). Phelan-McDermid syndrome does not have a specific treatment. The focus of treatment is on addressing the symptoms while also thoroughly screening for any related diseases. New therapies for this condition are now being tested in clinical studies.
63 years
Normal
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.
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.
The average height for someone with Morquios syndrome will grow an average of four feet. The life expectancy can vary from four years to seventy years.
a good long life
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.
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.
This condition would have no impact on life expectancy.
There's no shortening of life expectancy. The condition is manageable throughout the sufferers life.
rarely more than 30