PGD

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PGD

abbreviation for
(Medicine) preimplantation genetic diagnosis; a technique using in vitro fertilization to ensure that a baby does not possess a known genetic defect of either parent. After genetic analysis of the embryos so formed, only those free of defect are implanted in the mother's womb
References in periodicals archive ?
In vitro fertilization and preimplantation genetic diagnosis.
Outcome of preimplantation genetic diagnosis of translocations.
Ethics of using preimplantation genetic diagnosis to select a stem cell donor for an existing person.
The scientists postulated that the single cell technique used in preimplantation genetic diagnosis would carry over to stem cell research and that the technique doesn't harm the embryos, "but we don't know that either is true," Doerflinger said.
For these couples, preimplantation genetic diagnosis [PGD] represents a better solution.
A survey of 4,005 people by the Genetics and Public Policy Center, based in Washington, DC, revealed that 61 percent approve of using preimplantation genetic diagnosis (PGD) to help a sick sibling, while 33 percent disapprove.
Referred to as "savior siblings," the babies "were born after a technique called preimplantation genetic diagnosis (PGD) was used to test embryos for a tissue match to the ailing siblings," continues the report.
At the crux of the alternative, therapy-oriented embryonic i screening is a procedure known as preimplantation genetic diagnosis (PGD).
explained that the groups were asked to discuss scenarios involving carrier testing, prenatal testing, preimplantation genetic diagnosis, gene transfer, and sex selection.
The study, published in the April 10th issue of the New England Journal of Medicine, suggests that preimplantation genetic diagnosis (PGD), which combines the newest genetic testing and in vitro fertilization (IVF), may be a useful option for families with a history of congenital malformations.
Development and validation of concurrent preimplantation genetic diagnosis for single gene disorders and comprehensive chromosome aneuploidy screening without whole genome amplification.