Preimplantation Genetic Testing for Aneuploidy
involves checking embryos for abnormalities in
the number of chromosomes.
PGT-M Preimplantation Genetic Testing
for Monogenic/single gene defects can
be performed to reduce the risk of having
an affected child. PGT-M involves testing
embryos created through in vitro fertilization
(IVF) and then transferring unaffected embryos.
PGT-SR is a genetic testing method used to
detect chromosomal structural abnormalities,
such as translocations or inversions, in embryos
before implantation.
PGT-M is used to screen embryos for monogenic disorders, while PGT-HLA identifies embryos compatible for tissue donation to a sibling with
a specific medical condition.
Both PGT-M and PGT-A take place together during preimplantation, before the embryo has implanted in the uterus to avoid the risk of passing on a genetic disorder to a child.
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