Sentence examples for soft marker from inspiring English sources

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Exact(5)

Little is known about the association of this soft marker aneuploidy in various ethnic groups.

The most commonly expressed roles were that of 'hawk' or 'dove' (or hard and soft marker).

The presence of a soft marker alone (eg, 'raised nuchal translucency') is insufficient evidence of DS; however, DS can be considered antenatally detected using EUROCAT guidelines in the absence of invasive testing if multiple clinical signs are present, and termination of pregnancies are indeed performed on this basis.

An anomaly was deemed to be "antenatally detected" if the date of detection of the exact, or a closely related, anomaly predated delivery or the date of detection of an antenatal soft marker related to the anomaly present at delivery predated the date of delivery.

The definition of 'antenatally detected' followed European Congenital Anomaly Surveillance System (EUROCAT) guidelines, determined by the earliest suggestion of the precise, or closely related, anomaly, or identification of an antenatal soft marker 'nearly 100% predictive' of the anomaly present at delivery.

Similar(55)

To investigate women's expectations of routine ultrasound and experiences when soft markers were discovered: what the disclosure meant, how it affected them, how they experienced the information given and why they did or did not choose amniocentesis.

However, 23% of the study participants stated that soft markers should be reported only after the woman has been counselled and given her consent [ 33].

A finding such as fetal hydronephrosis range from being a soft markers or mild anomaly, to a serious condition associated with neonatal morbidity and mortality.

Inclusion criteria included patients of first degree Japanese ancestry, estimated gestational age between 14 and 24 weeks, and a finding of EIF regardless of presence or absence of other "soft markers".

While associated soft markers may be suspected during the initial booking scan, the majority of cases have historically been diagnosed following later uptake of blood tests or more invasive procedures.

Prognosis highly dependent on the results of an invasive test (e.g. omphalocele, bilateral clubfoot with chromosomal soft markers), or a reliable diagnosis was not available at inclusion due to an incomplete ultrasound examination (e.g. maternal obesity).

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