Genetic Testing for Future Parents offers genetic carrier screening to identify potential inherited genetic conditions that could be passed to children. This testing helps individuals and couples understand their risk of transmitting genetic disorders, enabling informed family planning decisions. By detecting gene mutations early, genetic testing provides valuable insights to ensure healthier pregnancies and mitigate the risk of passing on conditions like cystic fibrosis, sickle cell anemia, or other hereditary disorders.
Genetic Testing for Embryos (PGT) involves preimplantation genetic testing to detect genetic abnormalities in embryos before transfer during IVF. This process screens embryos for chromosomal issues or specific genetic disorders, helping ensure only healthy embryos are implanted. PGT enhances the chances of a successful pregnancy, reduces the risk of miscarriage, and helps prevent the transmission of inherited genetic conditions, offering prospective parents peace of mind in their family-building journey.
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