PGD Cancun

pgd-cancun

Pre-implantation Genetic Diagnosis (PGD) is a leading-edge, extremely detailed fertility treatment being used in IVF clinics in Cancun to diagnosis abnormalities in embryos.

Genetic testing and advanced assisted reproduction have united to introduce a powerful defense— preimplantation genetic diagnosis Cancun. This technology allows intended parents to choose which embryos to implant based on genetic testing outcomes.

IVF Cancun implements a progressive setting for PGD, both by technical modernization and clinical success rates, to aid a wide variety of intended parents to have healthy pregnancies.

Good Candidate for PGD Cancun

PGD testing may be appropriate for couples with:

  • Advanced maternal age (>36)
  • Experience of repeated miscarriage
  • Experienced repeated IVF failure
  • Previously pregnancy with a chromosomal abnormality
  • Risk of passing a genetic disorder on to their children
  • Risk of having children with a particular X-linked disorder
  • A partner who carries a balanced chromosomal translocation

PGD Procedure

Patients who are at risk for producing embryos with specific genetic abnormalities can find comfort with our PGD Cancun procedure.  PGD Cancun involves embryo biopsy including the removal of a single cell from an embryo on Day 3 of growth.

The embryo biopsy is executed by our IVF Cancun embryologists. Results are available within 24 hours; the embryos that are determined to be chromosomally and or genetically normal are then transferred on Day 4.

PGD Cancun is also successfully implicated for gender selection purposes.

Genetic Analysis with PGD

Chromosomal aneuploidy —

Chromosomal aneuploidy refers to an abnormality of chromosome number within the cells of the embryos.  Chromosomal irregularities may involve errors that occurred during cell division. Aneuploidy testing screens for common irregularities involving chromosomes X, Y, 13, 15, 16, 18, 21 and 22. This testing may be right for couples with advanced maternal age, couples with repeated miscarriages, couples experiencing repeated IVF failure, and couples who have previously had a pregnancy with a chromosomal abnormality.

Chromosomal translocations —

Chromosomal translocations encompass redisposition of the chromosomal material. Individuals who are carriers of a translocation may experience trouble with reproduction because they are producing chromosomally unbalanced embryos. The translocation may be the cause of an exertion conceiving, or may result in miscarriage after conception.

Single gene disorders —

Single gene disorders are genetic inheritable circumstances caused by the alteration or mutation of a specific gene located on one of the chromosomes. Individuals who are affected by one of these disorders, or who have a family history of a genetic disorder, may be at risk for passing the condition onto their children. Single gene disorders include cystic fibrosis, sickle cell anemia, Tay Sachs disease, and Fragile X syndrome.

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