Pgd & Gene Therapy - Should It Become a Normal Practice in the Nhs?

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Pre-implantation Genetic Diagnosis and Gene Therapy – Should it become normal practice in the NHS? PGD is a laboratory procedure that is used in conjunction with IVF (in vitro fertilization) to help detect certain diseases. Families affected by essentially any inherited disease can reduce the risk their offspring will suffer that genetic disorder by working with an experienced PGD team. Even families in search of a bone marrow donor may be able to use PGD to bring a child into the world that can provide matching stem cells. Gene therapy is the use of DNA as a pharmaceutical agent to treat disease. It originates its name from the idea that DNA can be used to enhance or alter genes within an individual's cells as a therapy to treat disease. PGD has many advantages - being able to test for more than 1,000 genetic conditions including Cystic fibrosis, Huntington's disease, Sickle-cell anaemia, Tay-Sachs disease and Down syndrome. This allows doctors to examine embryonic cells for certain genetic and chromosomal disorders and lets parents make implantation decisions based on the results Adults who know that they are carriers of a genetic disorder can undergo PGD to ensure their children won’t inherit the disorder meaning that if the disease you carry requires treatment throughout the course of your life, it may save you a small fortune because even though it costs a lot to have the PGD test it will save you a great deal in the long term. Parents can focus on specific areas of DNA involved in any conditions the parents may have doubts about. There will be a reduced risk of miscarriage when using PGD as only embryos without chromosomal abnormalities that can currently be detected through the procedure are implanted into the uterus. Therefore parents are less likely to be faced with the decision of having to have an abortion. Knowing which embryos are most

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