Is a newly established technique; its fundamentals is a genetic diagnosis of embryos before they are transfered into the uterus. This technique is actually a diagnostic test of elimination of known genetic disorders or chromosomal abnormalities. Diagnosis is carried out after a biopsy of one or two cells of an eight-cell embryo. These cells are consequently genetically tested.
Embryo is not damaged by this procedure in any way as at this point, each cell, at this stage, is capable of an individual development. Most frequent indications for pre-implantation genetic diagnosis are: chromosomal disorder of one of the parents, birth of a child with a hereditary disease, woman’s advanced maternal age, past unsuccessful IVF cycles and recurrent miscarriages.
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