it is on gene 8
the gene name is RECQL4
No. Triple X occurs on the sex chromosomes.
Patricia Ann Jacobs(1934-)has Triple X Syndrome. She is the first lady diagnosed Triple X. She is studying genetics now.
Triple X syndrome is a genetic mutation characterized by the presence of an additional X chromosome in females, resulting in a karyotype of 47,XXX instead of the typical 46,XX. It is considered a numerical chromosomal abnormality, where the extra X chromosome can lead to various physical and developmental differences, though many individuals with this condition are asymptomatic.
abstinance
Nondisjunction
The fragile X syndrome is a genetic disorder caused by mutation of the FMR1 gene on the X chromosome.
Barth syndrome occurs when a person is born with a mutated, or abnormal, TAZ1 (or G4.5) gene. This abnormal gene is located on the X chromosome, which is a sex-determining chromosome. Males have one X and one Y chromosome, while females have two X chromosomes.
No, they are two different things. Normally, a woman has 46 X chromozomes. If there are only 45 of them, it´s the Monozomy X, so called Turner syndrome. If there are 47 of them, it´s the Trizomy X, also known as the Triple X syndrome.
chromosome 21
There are no famous individuals known to have Triple X syndrome (also called Trisomy X). Triple X syndrome is a genetic condition that affects females where they have an extra X chromosome (XXY) instead of the typical XX combination. It is a relatively rare condition and may often go undiagnosed.
i dont think so but there might eventually. the above response is incorrect. Triple X syndrome does not have a treatment because you cannot take an X chromosome away from every cell in the body
The syndrome is caused by a severe change (mutation) in the HPRT gene . Since the HPRT gene is located on the X chromosome, Lesch-Nyhan syndrome is considered an X-linked disorder and therefore only affects males.