Rare Disease Forum by Genetidoc Genetic Clinic › Forums › Genetics in Pregnancy and Fertility › Soft Markers on Ultrasound › What is the outlook for soft markers on ultrasound, and will this marker affect
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Genetic Counselor.
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September 5, 2026 at 9:28 am #826
Anonymous
ModeratorWhat is the outlook for soft markers on ultrasound, and will this marker affect my baby after birth?
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September 5, 2026 at 9:31 am #827
Genetic Counselor
KeymasterFor the great majority of pregnancies, an isolated soft marker has no lasting significance at all. The marker itself, separate from any question about chromosomes, usually behaves as follows:
• Echogenic intracardiac focus Almost always disappears or becomes undetectable by the third trimester and has no effect on how the heart functions, before or after birth.
• Choroid plexus cysts Typically resolve by around twenty-six to twenty-eight weeks of pregnancy and, when isolated, are not associated with any developmental or neurological problem in childhood.
• Mild urinary tract dilation Usually improves during pregnancy or in the months after birth; a minority of babies are monitored briefly by a pediatric urologist after delivery as a precaution, without any impact on long-term kidney health.
• Thickened nuchal fold, shortened long bones, or absent nasal bone These are simply variations in measurement and, when isolated and unconnected to any chromosome or structural finding, do not predict any problem with growth or development.
• Single umbilical artery When isolated, growth is typically monitored a bit more closely later in pregnancy with an additional ultrasound or two, since a small increase in the chance of lower birth weight has been described, but the finding itself resolves nothing after birth, since the cord is no longer needed.The bigger-picture outlook, in other words, comes down almost entirely to whatever screening or diagnostic testing accompanies the finding, not the soft marker itself. A soft marker paired with reassuring screening carries an excellent outlook. If a chromosome condition is ultimately diagnosed, whether through screening that prompted diagnostic testing or through diagnostic testing pursued for another reason, the outlook then depends on that specific condition, and referral to a genetic counselor is recommended to discuss what is known about it. For the vast majority of families who encounter a soft marker on a routine scan, however, it becomes a passing note in the pregnancy record rather than something requiring any monitoring after birth.
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