Assisted Reproduction - Thrive IVF Fertility
Genetic Screening
Looking to balance your family and/or minimize the risk of passing on genetic conditions?
Thrive IVF is here to assist you.
Genetic screening is a crucial test when seeking infertility treatment because it can identify genetic factors that may contribute to infertility, recurrent miscarriages, or other reproductive challenges.
By detecting specific genetic abnormalities or inherited conditions that could affect fertility, genetic screening helps healthcare providers tailor treatment plans to address these underlying issues. It also allows prospective parents to understand the risk of passing on genetic disorders to their children, enabling them to make informed decisions about reproductive options, such as in vitro fertilization (IVF) with genetic testing of embryos.
Ultimately, Genetic Screening
Enhances the chances of a successful pregnancy and the birth of a healthy child by providing a clearer picture of potential genetic influences on fertility.
For more information about genetic screening and to schedule an appointment with Dr. Shaurin Patel at Thrive IVF Fertility, please call our Oklahoma City offices at 405-930-3483 or use our online contact form.
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Frequently Asked Questions
1. What is genetic screening in fertility care?
Genetic screening involves testing either prospective parents or embryos to assess the risk of inherited genetic conditions, chromosome abnormalities, or certain diseases that could affect a future child’s health. It helps couples make informed decisions about family planning and fertility treatments.
2. How does genetic screening work with IVF?
In IVF, embryos created in the lab can be biopsied and tested using preimplantation genetic testing (PGT) to evaluate chromosome number or specific genetic conditions before transferring them into the uterus, helping select embryos with the best chance for a healthy pregnancy.
3. Who should consider genetic screening?
Genetic screening is often recommended for couples with a family or personal history of inherited diseases, recurrent miscarriages, multiple failed IVF cycles, or advanced reproductive age. It’s also useful for individuals who want to better understand their risk of passing on certain genetic conditions.
4. What types of genetic screening are available for embryos?
There are different types of preimplantation genetic testing, such as PGT-A (for chromosome count abnormalities), PGT-M (for specific genetic disorders), and PGT-SR (for structural chromosome rearrangements), each designed to evaluate embryo health in specific ways before transfer.
5. Are there risks or limitations to genetic screening?
While genetic screening helps identify embryos with chromosomal or genetic issues, it isn’t a guarantee of pregnancy or a health outcome. Some embryos may not survive the biopsy process, and not all genetic conditions can be detected, so counselling with fertility specialists and genetic experts is recommended.