Almost every individual carries a gene for at least one genetic disorder. Genetic Carriers of Disease are individuals that have a mutation in a set of gene(s) that encode for a disease but have no signs of the disease themselves. Most screenings are to determine recessive disorders in both partners, to see if any disease-causing mutations can be passed on to their offspring. Persons known to be a carrier for a specific disease causing genetic disorder can then select to have their embryos tested for the disease before pregnancy is achieved.
Carrier Blood Tests are for:
Persons looking to freeze eggs
Persons looking to freeze sperm
For patients with a family history of a known disease-causing genetic disorder
For patients who already have a child with a known disease-causing genetic disorder
For patients diagnosed with certain types of cancer
The process,
explained simply.
Blood or Saliva Sample
A sample of blood, saliva, or tissue from the inside of your cheek will be tested. Typically, one partner who is more likely to be a carrier will be tested first.