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.
yes
The fragile X syndrome is a genetic disorder caused by mutation of the FMR1 gene on the X chromosome.
Fragile X Syndrome
Fragile X Syndrome
Fragile X Syndrome
Fragile X Syndrome
Fragile X Syndrome
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.
No, fragile x syndrome is not progressive
Martin Bell Syndrome.
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.
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.