IVF Risk of Birth Defects - What to Do

The vast majority of IVF babies are born normal andmissing pairs or have one extra copy. PGD can test
grow up healthy. While the IVF risk for geneticseveral chromosomes for disorders, but not all 23
defects is small, it increases with the age of thepairs. Another issue with PGD is that it can be
mother.inaccurate. There have been instances where healthy
The good news is that genetic defects in IVF-bornembryos have been considered abnormal by PGD or
babies can, for the most part, be prevented throughwhere abnormal embryos were considered healthy.
the help of embryo screening techniques. EmbryoThis is also the result of the test's limitations - even if
screening looks at a cell sample of an embryo for theone cell is tested normal, there is a chance that the
presence of chromosomal abnormalities that carryother untested cells may have undetected abnormal
genetic disorders like Beckwith-Widemann Syndrome,chromosomes. Comparative genomic hybridisation
Down 's syndrome, even certain types of cancer. It(CGH)
is not a perfect process and it cannot detect allA new approach called comparative genomic
conditions, but if you are over 35 and consideringhybridization (CGH) can be added to a PGD
IVF, embryo screening is something to seriouslyprocedure for more accurate results. It is more
consider. Pre-implantation genetic diagnosis (PGD) todifficult to perform and takes longer to complete but
Reduce Riskunlike a standard PGD, a CGH can identify genetic
Pre-implantation genetic diagnosis (PGD) was firstdisorders in all 23 chromosomes. Like in a standard
introduced to the public in 1987 to help couples avoidPGD, a blastomere is collected from the cell during cell
embryos with a particular genetic disorder. PGD wasdivision. Before examining the cell for genetic
initially restricted to those couples who are carriers ofconditions, a labeled identical copy of each
a potentially-life threatening genetic condition, butchromosome found in the cell is made. These DNA
most clinics now offer the procedure to anyone whocopies are then matched up or hybridized with labeled
wants to avail of it. IVF patients who are older thancopies of DNA from a different but normal cell. The
38, and who have had subsequent miscarriages orsample DNA and normal DHA are each labeled by
failed IVF cycles can benefit from PGD.certain colors, which are then analyzed by a
PGD is typically performed after fertilization, whencomputer program. Test cells that contain the normal
the embryos are anywhere between the four andnumber of chromosomes have the same color
ten-cell developmental stage. A single blastomereintensity as the normal cell. Test cells with too many
(cell) or two is gently removed from the embryochromosomes have a higher color intensity, while test
using nanosurgical techniques, and analyzed for thecells with too few chromosomes have a lighter color
presence of specific conditions. Only embryos withoutintensity.
these disorders are transferred into the uterus. AsideSmall clinical trials suggest that CGH can increase the
from guaranteeing the health of your baby, PGD alsosuccess of IVF by about 25%. Make an informed
increases the chances of carrying a pregnancy todecision About IVF Risks
term because it filters out embryos with an abnormalThese approaches are very useful and they can
number of chromosomes. Chromosomal abnormalitiesincrease your chance of a successful IVF. However,
are the leading cause of miscarriages because theykeep in mind that they do not absolutely guarantee
are unable to implant and develop normally.accurate results. There is a slim chance that genetic
Even though PGD can be used to identify a numberdefects and abnormalities can occur in babies with
of disorders, it cannot identify every single one. Anormal karyotypes, or chromosome profile. Do your
normal, healthy embryo has 23 chromosome pairs,research carefully and think about whether these
and certain disorders like aneuploidy may havepromising procedures are the best route for you.