What is the life expectancy of fragile x syndrome

what is the life expectancy of fragile x syndrome

Data and Statistics on Fragile X Syndrome

2 answers. Next. Individuals have a normal life expectancy. Some individuals with FX have seizures and connective tissue disorders. Carriers can have reproductive issues such as premature ovarian failure, tremor disorder called Fraxtas. Nonof these seem to endanger life expectancy except FXTAS. Jan 28,  · Life expectancy for people with fragile X syndrome is generally normal. Many affected people participate in an active lifestyle and have good health. Some people are more prone to a number of medical problems, such as ear infections and/or seizures. Regular medical checkups and awareness of increased health risks may improve the outlook for affected people.

World map of Fragile X Syndrome View more. What is the life expectancy what is onset of blood lactate accumulation someone with Fragile X Syndrome? Individuals have a normal life expectancy.

Some individuals with FX have seizures and connective tissue disorders. Carriers can have reproductive issues such as premature ovarian failure, tremor disorder called Fraxtas. Posted Aug 21, by m0mskie Translated from spanish Improve translation. Have a life expectancy equal to the rest of the people without disabilities. Posted Mar 3, by Maria Jose Fragile X Syndrome life expectancy Your answer Posting your answer Connect with them and share experiences.

Join the Fragile X Syndrome community. View map. Aged 20 after a family history of Fragile x and pregnant I was requested to take the fmr1 test which I did to discover I am a carrier my daughter now aged 20 was recently tested and found NOT to be a carrier.

In I became pregnant again with my Views: MY SON. When my son was 18 months old, it was decided that he was globally delayed in his development. A steep learning curve began. We were advised to conta Tell your story and help others Tell my story. Ask a question and get answers from other users. Ask a question. Find your symptoms soulmates From now on you can add your symptoms in diseasemaps and find your symptoms soulmates. Symptoms soulmates are people with similar symptoms to you.

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Life Expectancy. Life expectancy is not affected in people with FXS because there are usually no life-threatening health concerns associated with the condition. Prevalence. There have been a number of studies aimed at determining the prevalence of FXS in males and females. 43 rows · May 12,  · Life expectancy for people with fragile X syndrome is generally normal. . Apr 22,  · According to research, around 44% of women and 10% of men having fragile X syndrome are able to attain a high level of independence as adults. The life expectancy of a patient with fragile X syndrome is thought to be the same as any other normal person. The prognosis also depends on the degree of the symptoms of this condition.

What is the long-term outlook for people with fragile X syndrome? How might fragile X syndrome affect people in adulthood? How might fragile X syndrome be treated? We hope this information is helpful. We strongly recommend you discuss this information with your doctor. If you still have questions, please contact us.

Please see our Disclaimer. National Institutes of Health. COVID is an emerging, rapidly evolving situation. Menu Search Home Diseases Fragile X syndrome. Back to List of Questions. Question Question. If a child might have had this disorder and was never diagnosed, how does it affect him or her in adulthood? Answer Answer. The following information may help to address your question: What is the long-term outlook for people with fragile X syndrome? Life expectancy for people with fragile X syndrome is generally normal.

Many affected people participate in an active lifestyle and have good health. Regular medical checkups and awareness of increased health risks may improve the outlook for affected people. While the life span of people with fragile X syndrome FXS is typically normal, there is very little information in the medical literature about adults with FXS. The effect of specific medical problems or associated complications on adults with FXS may vary because not all affected people have the same features.

While affected males usually have moderate to severe intellectual disability , one third to half of affected females have average intellectual function. Because of this, some adult women with FXS may have very normative adult lives, including living independently; having a spouse or romantic partner; pursuing higher education; holding full-time jobs; having friends; and participating in a range of leisure activities.

Adult men with FXS are more likely to have much more limited independence. However, there are likely considerable differences between all people with FXS. Adults with FXS who also have an autism spectrum disorder diagnosis may have more limited independence in adult life than those with FXS only.

There is no specific treatment available for fragile X syndrome. References References. Fragile X Research Foundation of Canada.

Exploring the adult life of men and women with fragile X syndrome: results from a national survey. Am J Intellect Dev Disabil. January, ; 1 FMR1-Related Disorders. Share this content:. Close Copy Link. You May Be Interested In. How to Find a Disease Specialist. Tips for the Undiagnosed. Support for Patients and Families. Tips for Finding Financial Aid. Help with Travel Costs. How to Get Involved in Research.

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