Fertility Docs Uncensored is hosted by Dr. Carrie Bedient from the Fertility Center of Las Vegas, Dr. Susan Hudson from Texas Fertility Center, and Dr. Abby Eblen from Nashville Fertility Center. In this episode, we explore the various genetic tests available for infertility patients, including carrier screening, prenatal testing, and testing done during IVF. We discuss why these tests are important, what they detect, and how they can influence family planning decisions. We give you answers to many questions you may have. What is expanded carrier screening, and what types of traits does it look for in prospective parents? How does being a carrier for recessive traits affect a child, and what is the probability of a child being impacted if both parents carry the same trait? Which traits are typically tested, and why are only severe conditions included? How can results from carrier screening influence decisions about pursuing IVF and embryo selection? What is NIPT testing, and how is it performed during pregnancy? What types of chromosomal abnormalities can NIPT detect, and when is this testing appropriate? How is genetic testing performed at the time of IVF, and what are the different tests available for embryos? What is PGT-A, and how does it assess chromosomal abnormalities? How do PGT-M, PGT-SR, and PGT-P tests evaluate for recessive traits, structural abnormalities, and conditions caused by multiple genes? How do these tests help couples make informed decisions about their reproductive options? What are the advantages of testing embryos before implantation compared to testing during pregnancy? How can understanding these genetic testing options reduce risks and improve outcomes for patients undergoing fertility treatments? Knowing the answers to these questions will help you decide which of these tests are right for you.