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Preimplantation genetic testing for monotonic disorders in transport service: comparison of a targeted testing versus a genome wide testing approach Beatriz Dias Master Program in Biochemistry 2021Supervisor
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How to fill out preimplantation genetic testing for

01
Discuss with your healthcare provider if preimplantation genetic testing is recommended for your specific situation.
02
Inquire about the specific genetic conditions being tested for during the procedure.
03
Undergo counseling to discuss the potential outcomes of the results and implications for future pregnancies.
04
Provide a sample of cells from the embryo for genetic testing.
05
Wait for the results of the genetic testing before proceeding with the embryo transfer process.

Who needs preimplantation genetic testing for?

01
Couples with a family history of genetic disorders or chromosomal abnormalities
02
Individuals with a known genetic mutation that could be passed on to their offspring
03
Women of advanced maternal age
04
Couples who have experienced recurrent miscarriages or failed fertility treatments
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Preimplantation genetic testing is used to screen embryos for genetic disorders before they are implanted in the uterus.
Couples undergoing in vitro fertilization may choose to undergo preimplantation genetic testing to screen embryos for genetic disorders.
Preimplantation genetic testing involves extracting cells from embryos created through in vitro fertilization and analyzing them for genetic abnormalities.
The purpose of preimplantation genetic testing is to identify embryos that are free of genetic disorders, increasing the chances of a successful pregnancy.
The results of the genetic testing, including any abnormalities detected in the embryos, must be reported.
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