answersLogoWhite

0

Yes. Fragile X is essentially the gene silencing of FMR1 protein, a protein important for the generation of certain nerve cells. When there is one copy with excess CpG repeats, the other chromosomal copy remains active.

User Avatar

Wiki User

16y ago

What else can I help you with?

Related Questions

Is fragile x syndrome controlled by a dominant allele?

yes


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 an example of a genetic disorder that is caused by insertion of extra codons in the X sex chromosome?

Fragile X Syndrome


What is an example of a genetic disorder that is caused by insertion of extra codons in x sex chromosome?

Fragile X Syndrome


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 an example of a genetic disorder that is caused by insertion of extra codons of the X sex chromosome?

Fragile X Syndrome


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

Fragile X Syndrome


How is Fragile X Syndrome Inherited?

Males and females can be carriers, male carriers can only pass on to their daughters, they will be carriers as well have a premutation. Females can pass on to their sons or daughters, they will have the premutation or the full mutation.


Does fragile X get worse?

No, fragile x syndrome is not progressive


What is the scientific name for Fragile x syndrome?

Martin Bell Syndrome.


Will a person with fragile x syndrome be able to live independently?

Fragile X, like autism, is a spectrum disorder, which could result in anything from mild learning disabilities to severe impairment. Individuals can live independently, with or without supports. I recommend the documentary "Living with Fragile X" if you have the opportunity to see it.


Is fragile x a x linked disorder?

Yes, Fragile X syndrome is an X-linked genetic disorder that causes a range of developmental problems. It is caused by a mutation in the FMR1 gene located on the X chromosome. The condition is more commonly seen in males than in females because they have only one X chromosome.