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| Blastocyst-stage embryo |
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| Human chromosomes in the cell |
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Special techniques
Extended culture of
embryos
In some circumstances, an extended period of culture (4 - 7 days)
can help in selection of the best embryo for transfer. A blastocyst
stage embryo provides a somewhat greater likelihood of pregnancy
compared with, for example, a transfer of a 4-cell stage embryo.
A good functional method for freezing human blastocyst has not been
develpoped yet, which affects the treatment options. It is worth
noting that only approximately 4 - 6 embryos out of ten reach the
morula stage when cultured. When there is a small number of embryos,
this method cannot yet be recommended as the first treatment option.
Assisted hatching
In the case where the transparent surface layer surrounding the
embryo (zona pellucida) is found in microscopic inspection to be
noticeably thicker and harder than normal, it is possible to help
the embryos to hatch with special techniques; by thinning or making
a hole in the zona. This type of thicker structure of the zona may
be the cause of infertility for some couples in that the normal
implantation of the embryos into the uterus has been disturbed or
obstructed.
Gene and chromosome
diagnostics based on the embryo.
A small number of couples may have singular genetic or chromosome
errors which cause infertility. These errors may be apparent both
in male and female gametes. Some of these errors may be detected
by examining the family medical history, but some are newly generated
and are discovered only when the couple in question is thoroughly
examined. In some cases, analyses of blood samples by both partners
can give information on the genetic background of infertility; in
some cases, singular gene tests can be done in order to determine
the causes of infertility. All gene and cromosome errors do not,
however, mean that the situation would be hopeless with respect
to the embryos: one only needs to find a healthy embryo for the
transfer!
A method called embryo biopsy followed by genetic
analysis of the embryo (PGD, preimplantation genetic diagnosis)
has been developed to solve this problem. Normally one or two biopsied
cells from an 8-cell stage embryo are analysed for suspected gene
or chromosome errors. After the analysis those one or two embryos
that prove to be normal with respect to the error in question are
selected for the transfer. This procedure can also be done later
by amniocentesis or placental villus biopsy, but at this stage the
fetus is already implanted in the uterus. The embryo biopsy techique
is in use in our clinic, but its use requires a specific, real need.
It is not possible to choose the sex of the embryo based on the
wishes of the parents only, for instance.
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