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Previous fetus/child with a congenital, genetic, or chromosomal abnormality
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Known or suspected fetal anomaly or growth disorder in current pregnancy
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Fetus at increased risk for a congenital anomaly, such as the following:
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Maternal pre-gestational diabetes, or gestational diabetes diagnosed before 24 weeks’ gestation
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Pregnancy conceived via assisted reproductive technology
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High maternal body mass index
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Multiple gestations
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Abnormal maternal serum analytes, including a-fetoprotein level and unconjugated estriol
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Teratogen exposure
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First-trimester nuchal translucency measurement of 3.0 mm or greater
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Fetus at increased risk for a genetic or chromosomal abnormality, such as the following:
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Parental carrier of a chromosomal or genetic abnormality
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Maternal age of 35 years or older at time of delivery
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Positive aneuploidy test, including non-invasive prenatal testing
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Soft marker for aneuploidy on ultrasound
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Other conditions affecting the fetus, including the following:
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Congenital infections
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Maternal drug dependence
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Alloimmunization or Isoimmunization
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Oligohydramnios or Polyhydramnios
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Suspected placenta PAC or risk factors for PAS such as placenta previa in the third trimester or a placenta overlying a prior Cesarean scar site