At the UCSF Center for Reproductive Health, we offer various genetic testing options tailored to your fertility needs, such as carrier screening, preimplantation genetic testing for monogenic disorders (PGT-M), and preimplantation genetic testing for aneuploidy (PGT-A). Carrier screening helps identify whether you or your partner are carriers of genetic variations that could heighten the risk of passing on genetic disorders to your child. Most of these inherited conditions follow an autosomal recessive pattern, meaning there’s about a 25% chance of having a child affected if both parents are carriers. We also test for selected X-linked conditions, primarily affecting sons born to carrier mothers, although both genders can exhibit symptoms.
The screening process involves a simple blood draw or saliva sample. Our genetic counselors, who are specially trained in both medical genetics and counseling, play a crucial role in this journey. They provide risk assessments, educational support, and help you navigate the complexities of genetic testing, interpreting results, and advocating for your needs.
If you’re interested in exploring more about fertility practices, check out this blog post on pause, pose, handstand, pike. It’s a fun read that adds to your understanding of fertility. For those considering home insemination options, the BabyMaker Home Intracervical Insemination Syringe Kit Combo is a great resource to explore. Don’t forget to also check out Johns Hopkins Fertility Center for more information on IVF and pregnancy support.
In summary, genetic screening and counseling are invaluable components of the fertility experience, offering insights and guidance as you make informed decisions about your family planning journey.