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What cause fragile X syndrome?

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Anonymous

13y ago
Updated: 3/26/2021

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

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Wiki User

16y ago

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Related Questions

Does fragile X get worse?

No, fragile x syndrome is not progressive


What is an examples of a genetic disorder that is cause by insertion of extra codons in the X sex chromosome?

Fragile X Syndrome


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


Does Cee-Lo Green have Fragile X Syndrome?

There is no public information or credible reports indicating that Cee-Lo Green has Fragile X Syndrome. Fragile X Syndrome is a genetic condition that affects intellectual abilities and can cause various developmental issues, but Cee-Lo Green has not disclosed any such diagnosis. His career as a musician and performer has been primarily focused on his talents in the music industry.


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


Is fragile-x-syndrome due to heredity or is it a mutation?

mutation