When most people think of DNA testing, Thalassemia is probably not the first thing that comes to mind. However, even for those that do not exhibit any symptoms, DNA carrier testing for Thalassemia is an important way to ensure that you do not unwittingly pass on this severe illness. But what is all of the fuss about? What is Thalassemia?
Thalassemia is a genetic blood disorder that causes the blood to make an odd kind of hemoglobin. Hemoglobin is the protein in red blood cells that allows for oxygen to be carried throughout your body. With Thalassemia, a large percentage of red blood cells are destroyed by the abnormal hemoglobin. This destruction of blood cells often leads to anemia.
That is how it works, but what about the symptoms? The most severe symptom of Thalassemia is a stillbirth, but there are other symptoms that those with Thalassemia may display. These includes:
This illness is clearly a severe one, so who should consider DNA carrier testing for Thalassemia?
If you have an interest in any of the following categories, it is important that you be tested for the Thalassemia carrier gene.
The good news is that testing is simple. Any doctor can perform a test with only one blood sample. However, it is important that the test examines three areas: complete blood count, iron studies, and hemoglobin electrophoresis. If all of these conditions are meant, it is a simple matter to determine if you possess the carrier gene.
It is incredibly easy to protect yourself and your family from this serious illness so long as you get tested. With such a simple testing procedure, there is no reason to not know your Thalassemia status. After all, who would want to sit in the dark about an illness like this?
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