answersLogoWhite

0

Yes. It is found as a mutation on the X chromosome (a sex chromosome) so it is sex linked. The gene for Fragile X is carried on the X chromosome. Because both males (XY) and females (XX) have at least one X chromosome, both can pass on the mutated gene to their children.

User Avatar

Wiki User

10y ago

What else can I help you with?

Related Questions

What are three diseases that are sex linked like hemoplilia?

Three disorders which are sex-linked are: Fragile X syndrome Duchenne muscular dystrophy Colour blindness (most forms, but not all)


Is Klinefelter Syndrome sex-linked or autosomal?

Klinefelter Syndrome is sex-linked, because it is a genetic defect that results in a male having an extra 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 an 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 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 in x sex chromosome?

Fragile X Syndrome


Does fragile X get worse?

No, fragile x syndrome is not progressive


How many chromosome do you have when you have fragile x syndrome?

Fragile X syndrome is caused by a mutation that prevents the Fragile X mental retardation (Fmr-1) gene from being transcribed. This gene is located on the X chromosome (the sex chromosome). Since males only carry one of these chromosomes, they are twice as likely to be affected by the mutation than females.


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.


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.


What are 2 human genetic diseases that have been linked to elongations of base triplet repeats?

Hunington's disease and Fragile X syndrome