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Our laboratory is proud to offer
Pre-Implantation Genetic Diagnosis with Fluorescent In Situ
Hybridization to test embryos for some chromosomal abnormalities,
X-linked diseases and sex selection for family balancing prior to embryo
transfer.
The South Florida Insitutute
for Reproductive Medicine is happy to announce it is a partner clinic of
Gene Security Network (GSN) furthering our commitment to bringing our
patients the most advanced reproductive technology options. GSN offers
preimpantation genetic diagnosis for aneuploidy (PGD) using microarray
and proprietary Parental SupportTM bioinformatics. GSN
screens all 24 chromosomes for aneuploidy and offers the most
accurate and comprehensive PGD results; no embryo freezing is required
GSN’s Parental SupportTM is the only technology available
that can detect parental source of aneuploidy, haploidy/polyploidy, and
uni-parental disomy. Learn more about
GSN’s PGD Expertise here.
As maternal age increases, the incidence of
chromosomal abnormalities rises resulting in decreased fertility and
increased risk of spontaneous pregnancy loss and live born infants with
chromosomal abnormalities such as Downs Syndrome. This treatment allows
the laboratory to remove embryos containing certain numerical
chromosomal defects (aneuploidy) from the pool of embryos available for
transfer. There is preliminary evidence to suggest that aneuploidy
screening in certain couples may improve the success of IVF by selecting
embryos which possibly have both an improved potential for implantation
and a decreased rate of spontaneous loss while also decreasing the
chance of a live born child with chromosomal abnormalities.
The eight chromosomes tested are 13, 15, 16, 18,
21, 22, X and Y. Though technically demanding, the testing has a low
error rate approximated at 2% to 5% by current data. |