Only chorionic villus sampling and amniocentesis can definitely detect or rule out
fetal genetic abnormalities, but these are invasive to the pregnancy and carry a risk of miscarriage.
Not exact matches
New research has found that routine screening using a non-invasive test that analyzes
fetal DNA in a pregnant woman's blood can accurately detect Down's syndrome and other
genetic fetal abnormalities in the first trimester.
Therefore, it is more than evident that
fetal structural malformations and other
fetal abnormalities revealed through prenatal ultrasound are characterized by considerable phenotypic and
genetic heterogeneity.
Similarly,
fetal limb deformities, such as structural
abnormalities of the fingers and toes (clinodactyly, polydactyly, etc.), are relatively frequent ultrasonographic findings and are also associated with a variety of syndromic and non-syndromic
genetic disorders (Warman et al., 2011; Porter & Herman, 2011).
After consideration and assessment for the risk of a
genetic abnormality, followed by a detailed ultrasound for
fetal anatomy, the pregnancy should progress as normal.