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Expanding understanding of genetic diseases.
BJOG : An International Journal of Obstetrics and Gynaecology 2020 September 27
As genetic technologies evolve, our understanding of the causes of fetal structural anomalies and related fetal genetic diseases will expand. This ability will no longer mean that with the discovery of a severe fetal anomaly the patient must decide to either terminate the pregnancy or risk having a child with potentially severe and lifelong difficulties, the extent of which can only be reliably elucidated postnatally. However, implementation of in-utero genomic testing now allows "precision fetal medicine" in which specific fetal diagnosis and prognosis are available.
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