Pgd Is Known As Pre Implantation Genetic Diagnosis

Preimplantation genetic diagnosis (PGD) is a form of genetic testing. It is similar to the screening of abnormal chromosome count only used to test for genetic diseases. The fertility institutes have used this to take gender selection to the next level. Stating that this has a greater than 99,9% success rate.

A Preimplantation Genetic Diagnosis (PGD) is a test that “allows future parents to detect genetic defects that cause inherited disease in human embryos before they are implanted.” One of the most ethical questions that one might ask before considering the PGD is whether the benefits of genetic knowledge outweigh harmful effects that occur to the embryo? Is it really worth manipulating embryos genes in order to achieve the desire of the parents? Often times we have to take into considerations the risk and benefits of each situation. I believe that the PGD test should be only be done to detect genetic defects, but it should not be used to manipulate genes in order to make what to them is a “perfect” child. As stated in our text, “ In the united Kingdom alteration of an embryos genes, even for gene therapy or cloning embryos is illegal.” By manipulating genes its like going against Gods wishes. In the eyes of God every person that comes into this world is equally seen as a human being because they are all created in “ the image of God.” In this case the parents should not be allowed to manipulate the genes of their unborn child just to accommodate to their

Embryonic tissue that was removed is first tested for genetic abnormalities. This is done so that the healthiest embryos are frozen and implanted. Dr. Timothy Yeko, a medical director of the assisted reproductive technology program at the Reproductive Medicine Group in Tampa, talked about the genetic testing, “ Most of our patients now choose to have this genetic testing, which has come into widespread use in the past year or so. By doing this , the miscarriage rate has dropped by 50 percent because the genetically abnormal embryos are the ones that end in miscarriage.”

PGD is known as pre-implantation genetic diagnosing. I do not think it is ethical to design and conceive a child that meets specific genetic requirements. I do not feel that this is an ethical reason to conceive a child. Rather, I believe all children should be seen as blessings or gifts, not sacrificial genetic progeny.

Therapeutic genetic manipulation is preformed by doctors to prevent diseases that the baby is carrying. The baby is tested by screening the embryo for any possible unknown diseases. Sometimes the PGD or preimplantation genetic diagnosis technique is used for this ("Biotechnology special focus"). The main diseases PGD is used to test for in babies are Hunntington's disease, Tay-sacks, Alzheimers, Familia cancers, Sickle Cell disease, Hemophilia, Neurofibromatosis, Fanconi's Anemia, Cystic fibrosis and most recently, Down's Syndrome ("Hooray for designer babies", 2002). This technique involves removing the unfertilized egg from the female, mating it with a sperm and then testing it for diseases. If all the diseases are absent, the fertilized egg is planted into the mother's uterus to develop into a baby. Some other unpredictable diseases may also be carried in the baby's chromosomes. Chromosome carrying diseases and disorders include: miscarriage of the baby, physical birth defects or down syndrome (Biotechnology special focus").

One advantage is the ability to reduce the risk for diseases. Through procedures like pre-implantation genetic diagnosis (PGD), one can inspect embryos created by in vitro fertilization (IVF) for many genetic conditions (Macklin, 2014, para. 1). While this process can be extremely beneficial ensuring the health of future generations, it can be misused in many ways.

Currently it is only legally possible to carry out two types of advanced reproductive technologies on humans. The first involves choosing the sperm to fertilize the egg, which will determine the sex and the genes of the baby. The second technique screens embryos for a genetic disease and only selected embryos are implanted back into the mother’s womb. This is called Pre-implantation Genetic Diagnosis (PGD).

Doctors have an important role in honor the patient’s autonomy by let them make their own decision in rather or not to have the embryos screen out for Tay-Sachs disease prior to fertilization. However, in this specific case we should also take in consideration the child’s best interest. The parents have already lost two children for the disease. As health care professionals we know that the couple still have a chance to produce an affected child since both of them are carriers. Therefore, we decided to do the Tay-Sachs PGD screening anyway, implant the healthy embryos and not disclose the fact that PGD was performed. In doing so the parents will have a chance to bear a healthy child who will have higher chance to have the best life possible.

The element of excitement when procreating offspring ceases with the development of Genetic Engineering. Parents will no longer wonder if their child will have grandma’s curly brown mane or Uncle Todd’s piercing gray gaze. The scientific breakthrough in technology of Pre-Implantation Genetic Diagnosis (PGD), originally created to screen diseases in embryos, has now become tantamount to an online shopping cart for determining cosmetic traits. To the parents who wish to decide what their children look like, you may be headed in the direction of becoming Adolf Hitler Lite. Using reproductive technologies to determine cosmetic features borders on scientifically useless and irresponsible, as it is basically a guise to revive eugenics.

Preimplantation Genetic Diagnosis (PGD) is a procedure used to identify genetic faults in embryos created with In-Vitro Fertilization. In the movie, GATTACA, PGD is the social standard. I disagree with the widespread use of PGD.

PGD is performed with IVF and followed by genetic screening for mutant gene. IVF stage, eggs are collected and fertilized by sperm in the laboratory to produce Zygotes. Then, these Zygotes carry on to growing in the laboratory for 3 days until reached eight cells stage. Biopsy of embryo is performed and extracted blastomere from each 6-8 cell stage embryo. Then, cell undergoes genetic screening for mutant gene. Un-carrier and unaffected embryos are transferred into mother’s uterus with confident no CF mutant gene for ensuring a quality of life for baby (Destouni, 2016).

A positive biological implication of PGD is if they seem to remove the allele from the DNA of the embryo, then the allele will not be present in the generations following.

Scientists have done a lot of research in the past decades concerning reproduction and developed a treatment called PGD. This treatment seems, for many people, to be the solution for almost everything that could go wrong with a human being, like illness, certain character traits, physical appearance and so on. However, others don’t think that good about it, it is unethical for them.

It can also be used to test for Tay-Sachs Disease, Fragile-X Mental Retardation, Cystic Fibrosis, Down Syndrome and Spinal Muscular Atrophy. In the past couples who wanted to have childr en, and were carriers of inherited diseases, worried about the possibility of their children inheriting the disease. Parents will no longer have this worry. In 1989, an English couple became the first to use PGD [Grady,1995]. It was used because they were at risk of passing along a form of severe mental retardation. Because it only affected sons, PGD was used to ensure that the couple had a daughter.

x PDG stands for Pre Implementation Genetic diagnosis it is a technique used to help examine and recognise a specific genetic defect within embryos created using IVF (In-Vitro Fertilisation). This technology is performed to prevent disorders or diseases being passed on to the child. The ultimate aim for couples attempting to use PGD is to produce an offspring free of chromosomal genetic defects. In New Zealand this technology is very limited and every application must be sought through and gain approval by the Ethics committee. Only specific severe conditions with a 1 in 4 chance of inheriting the disease are considered to carry out this process.