Understanding The Causes And Complications Of Turner Syndrome

Turner syndrome is a genetic condition! It is the result of a compromised or missing X chromosome. This condition appears in women and not men, because women are born with two X chromosomes. Turner syndrome patients will only have one working X chromosome! The condition varies between patients, as it depends on what parts of their chromosomes are missing. It is often diagnosed when patients are born. If not, it is caught early in their childhood!

Turner syndrome causes many physical and developmental issues. Thankfully, there are many options for Turner syndrome treatment! Individuals receive growth hormone therapy for Turner syndrome. This is crucial for their thyroid! Estrogen therapy for Turner syndrome is vital for patients to begin puberty. Of course, individuals need a variety of Turner syndrome specialists to manage all of their symptoms. This team varies over time as their symptoms change. They are essential for symptom management as well as dealing with Turner syndrome complications!

Genetic Abnormalities

Turner syndrome occurs when one of a woman's X chromosomes is compromised! One healthy X chromosome will perform the needed genetic functions. However, the other one has a compromised structure! Part of the genes will be missing. They will also function abnormally! Certain Turner syndrome patients even have no second X chromosome. In fact, they account for fifty percent of all cases of this condition!

The genetic abnormalities only occur in some cells for certain patients. This means that some of their cells will have two working X chromosomes. When this happens, it is called mosaic Turner syndrome. It is also worth noting that more research must be done on this condition. Doctors need to determine which chromosomes have the most significant influence on the symptoms of this condition!

Get the details on Turner syndrome complications next!