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What You Should Know About Preimplantation Genetic Testing

Every woman’s dream of getting pregnant, carrying the baby for nine months, and giving birth to a healthy baby can become a reality. However, some women have a problem carrying a pregnancy which, in the worst case, ends up being a miscarriage. This is very sad as every woman desires to carry their pregnancy up to giving birth. Miscarriage has led to broken marriages and homes since very little information is known concerning it. For this reason, doctors and other medical experts have developed new techniques for handling miscarriages. Newport Beach preimplantation genetic testing offers more information regarding miscarriage treatment. Please book an appointment to learn more.

What is preimplantation genetic testing?

This is a testing service that helps women reduce the chances of miscarriages. It is an elective service to all in vitro fertilization patients. This testing service is most effective for women under 35 years who have unexplained infertility issues. The most appropriate time for performing this test is during the blastocyst stage, occurring around seven days after the fertilization process. Preimplantation genetic testing has the following two options:

·   Comprehensive screening of the chromosomes

·   Preimplantation genetic diagnosis

As the patient waits for the biopsy results, doctors usually freeze the embryo. The freezing makes it ready if the results confirm the embryo is healthy. This testing does not affect the likelihood of successful in vitro fertilization.

What is comprehensive chromosome screening?

It is also referred to as preimplantation genetic screening. The screening mainly checks whether the embryo has the correct number and type of chromosomes. An embryo should have 23 pairs of chromosomes, one pair from the mother and the other pair from the father. If there is a difference in the number of chromosomes or different types of chromosomes being present, it can cause pregnancy complications. The complications can also affect the general health of the unborn child. As suggested by medical practitioners, the best candidate for this screening is women below the age of 35. Patients with the following factors are also considered:

·   If a woman has a history of recurrent miscarriages.

·   If the woman has irregularities with ovarian functioning.

·   If an individual is interested in embryo banking.

·   If a patient has a history of failed fertility treatments.

Before it is transferred to the uterus, screening of the embryo assures of high chances that a woman will carry her pregnancy until the time of giving birth.

What is a preimplantation genetic diagnosis?

Preimplantation genetic diagnosis is primarily used to check for any signs of genetic disorders that affect the pregnancy. The most suitable candidates for this diagnosis are carriers of genetic disorders, such as muscular dystrophy and cystic fibrosis. The test helps medical practitioners identify an embryo that is not affected by these genetic disorders, hence assisting in preventing transferring the disorders to the unborn child.

In conclusion, miscarriage is difficult to handle, especially if a woman has long been waiting for a child. Any individual who has experienced multiple miscarriages should visit a hospital immediately to receive screening to help save their pregnancy.