CGx testing, or carrier screening, is a preventative genetic test that looks for specific mutations (changes) in a person’s genes. A CGx test can help identify:
* People who carry one copy of a mutation and could pass it on to their children; and
* People who don’t carry the mutation and don’t have a risk of passing it on to their children.
CGx testing can be done by analysing the DNA in a sample of blood, saliva or hair roots. The test is usually carried out for adults who are considering having children (or before they start trying) but may also be appropriate for some people who already have children. CGx tests are available for a number of different conditions, including cystic fibrosis, Tay-Sachs disease and sickle cell anaemia. Most CGx tests are offered through commercial companies, but some NHS trusts also offer them. A CGx test is recommended for adults who are considering having children. The test can help to identify people who carry a mutation that could be passed on to their children.
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