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• W320293925 abstract "Recent developments in circulating cell-free nuclei acid screening and microarray assays have changed our fundamental approach to prenatal diagnosis, which had been based on relatively crude screening algorithms geared to the detection of fetal chromosomal abnormalities and a limited number of Mendelian disorders. We now see a far more effective approach to screening for common fetal aneuploidies and have begun to change our focus from chromosomal and Mendelian disorders to the expansive number of genomic deletions and duplications, many of which are associated with clearly defined clinical presentations. Regardless of the new advancements being introduced into clinical care, the diagnosis of fetal chromosome and genomic abnormalities is still only achievable by invasive prenatal diagnosis. In this chapter, we present current information on the techniques, effectiveness and safety of amniocentesis and chorionic villus sampling (CVS), as well as other fetal diagnostic procedures that are used less frequently because the advancements of the Human Genome Project have allowed for the diagnosis of an increasing number of conditions by CVS and amniocentesis rather than fetal tissue biopsy. Until a method is developed to reliably obtain fetal cells from maternal blood, invasive prenatal testing will likely remain an integral part of obstetrical care." @default.
• W320293925 created "2016-06-24" @default.
• W320293925 creator A5039806141 @default.
• W320293925 creator A5068208059 @default.
• W320293925 date "2013-01-01" @default.
• W320293925 modified "2023-10-10" @default.
• W320293925 title "Techniques for Prenatal Diagnosis" @default.
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