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there is no cure for fragile X syndrome. Management includes such approaches as speech therapy, occupational therapy, and physical therapy. The expertise of psychologists, special education teachers, and genetic counselors

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What is the treatment for fragel x syndrome?

A treatment plan for fragile X syndrome is tailored to the patientâ??s specific needs. Common treatments are: special education, speech and language therapy, occupational therapy, and medication.


Does fragile X get worse?

No, fragile x syndrome is not progressive


Why is there no treatment available for fragile x syndrome?

there is no cure because no one is smart enough to find one


What cause fragile X syndrome?

The fragile X syndrome is a genetic disorder caused by mutation of the FMR1 gene on the X chromosome.


What is the scientific name for Fragile x syndrome?

Martin Bell Syndrome.


What is the life expectancy of a person with fragile x syndrome?

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


By what other names is fragile X syndrome known?

also known as Martin-Bell syndrome, Marker X syndrome, and FRAXA syndrome


Who was the founder of fragile x syndrome?

Martin bell


How many people have fragile x syndrome?

4


Can a non repeat mother with out fragile x syndrome pass it to her male offspring?

A non-repeat mother without fragile X syndrome cannot pass the condition to her male offspring. Fragile X syndrome is caused by mutations in the FMR1 gene, specifically the expansion of CGG repeats, which typically occurs in carriers with a certain number of repeats. Since the mother does not have the syndrome or carry the premutation, her male offspring would not inherit the genetic mutation associated with fragile X syndrome.


Why chromosomal analysis is needed for bone marrow and fragile X-syndrome determination?

"Chromosomal analysis" should not be used for Fragile X Syndrome determination. Chromosomal analysis, Karotyping, has proven unreiable in diagnosis. Detemination can be made through DNA testing for Fragile X Syndrome, FMR1 DNA test.


What ethnic group is more likely to get Fragile X syndrome?

affects males and females of all ethnic groups. It is estimated that there are about one in 4,000 to one in 6,250 males affected with fragile X syndrome. There are approximately one-half as many females with fragile X syndrome as there are males