In the United States, all states require that newborns be tested for certain genetic and metabolic abnormalities that cause specific conditions. This is the most common type of genetic testing. Newer testing called cell-free DNA testing looks at a baby's DNA via a blood test done on the mother. Traditionally this is done looking at markers in blood or by invasive testing such as amniocentesis. Down syndrome and trisomy 18 syndrome are two genetic disorders that are often screened for as part of prenatal genetic testing. If you're pregnant, tests can detect some types of abnormalities in your baby's genes. If you have a particular health condition or disease, this type of genetic testing may help determine what medication and dosage will be most effective and beneficial for you. An expanded carrier screening test can detect genes associated with a wide variety of genetic diseases and mutations and can identify if you and your partner are carriers for the same conditions. If you have a family history of a genetic disorder - such as sickle cell anemia or cystic fibrosis - or you're in an ethnic group that has a high risk of a specific genetic disorder, you may choose to have genetic testing before having children. For example, this type of test may be useful for identifying your risk of certain types of colorectal cancer. If you have a family history of a genetic condition, getting genetic testing before you have symptoms may show if you're at risk of developing that condition. Presymptomatic and predictive testing.For example, genetic testing may be used to confirm a diagnosis of cystic fibrosis or Huntington's disease. If you have symptoms of a disease that may be caused by genetic changes, sometimes called mutated genes, genetic testing can reveal if you have the suspected disorder. Different types of genetic testing are done for different reasons:
Genetic testing plays a vital role in determining the risk of developing certain diseases as well as screening and sometimes medical treatment.
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