Genetic disorders and diseases
Genetic disorders and diseases Genetic disorders are caused by changes in the DNA structure, that disrupt body function. Our body’s cells function thanks to the proper activity of genetic material, this means that even the slightest defect can cause a genetic disease. Since genetic disorders harm the DNA itself, they usually cause extensive disturbances to […]
Maternal blood screening – prenatal maternal blood tests (non-invasive prenatal testing)
During the pregnancy, it is highly important to detect and diagnose genetic diseases in the fetus as early as possible. These diseases may be serious, which could lead parents to debate whether they wish to terminate the pregnancy or continue it, according to their personal choices and beliefs, and according to the severity of the […]
Types of genetic testing
There are many different types of genetic tests for identifying genetic diseases and defects. The scientific basis for all these tests is similar – identifying defects in the DNA. However, there are certain differences between the tests, such as in the resolution of defect identification, price range and accessibility. Certain tests are condition-specific, and are […]
Futura Genetics test
Futura Genetics test There are many medical conditions known to have a genetic cause. Knowing our risk for developing certain conditions can help us adjust our lives accordingly and lower these risks. Futura Genetics is an innovative non-invasive DNA test that can provide information on the risk of developing 28 genetic diseases. What diseases […]
First trimester screening – Genetic tests in the first trimester
First trimester screening – Genetic tests in the first trimester First trimester prenatal screening is a series of procedures performed during the first trimester of pregnancy to determine if the baby may be born with genetic defects. Most of these tests are noninvasive. Genetic tests indicate possible risks and probabilities of a certain medical abnormality. […]
CGH testing – Comparative genomic hybridization – biochip testing
Comparative genomic hybridization (CGH) is an innovative genetic test that detects small-scale changes in the DNA that can cause genetic disorders. The test is recommended in cases of a risk for genetic disorders, such as in children with intellectual impairment or during the pregnancy when fetal development delays are detected. Biochip testing is based in […]
