No, fragile x syndrome is not progressive
This particular karyotype has 45 chromosomes (instead of the usual 46). "XO" tells us that the karyotype is missing a sex chromosome: the individual has an X, but no homologous sex chromosome (X or Y) to complete the diploid pair.
Fragile X is a result of a mutation in the FMR1 gene on the X chromosome.
A biological male.
It is called a karyotype. If it shows two X chromosomes, the person is a female; if it shows one X and one Y chromosome, the person is a male.
The fragile X syndrome is a genetic disorder caused by mutation of the FMR1 gene on the X chromosome.
The question is not really clear. A karyotype is the overall complement of chromosomes isolated from a cell or organism (eukaryotic). When the karyotype of a normal healthy female is prepared for viewing by a cytogeneticist, there are 22 pairs of autosomal chromosomes present (ie two of chromosome 1, two of chromosome 2 etc...). There is one additional pair of sex chromosomes (two copies of X). A normal healthy human male also has 22 pairs of autosomes but the pair of sex chromosomes is not matched but instead there is one X chromosome and one Y chromosome (which is smaller than the X). So, if you look at a karyotype that has been laid out - if the two sex chromosomes are different sizes (X and Y) then the karyotype is from a male, if however they are the same size (X and X) then the karyotype is from a female.
A karyotype.
A karyotype will do that.
yes
A karyotype is a visual display of the chromosomes arrangeed by size, shape, and banding pattern.
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