Evidence map›Paper›PMID 41218004›Full record

ArticleFetal diagnosis and therapy2026

Low-Set Ears: A New Marker of Fetal Chromosomal Anomalies.

Elisabet Baldrich-Martin, Gloria Jalencas, Isabel Mazano, Cristina Lesmes-Heredia, Josep-Maria Manresa-Dominguez, Maria Iniguez-Cruz, Joan-Carles Ferreres, Viviana Beltran, Antoni Borrell

Abstract readMulticenter Study
In one paragraph

Article in Fetal diagnosis and therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

9 authors.

Elisabet Baldrich-MartinObstetrics and Gynecology Primary Care Center (ASSIR) Sabadell, Inst,tut Catala de la Salut, Barcelona, Spain, dbaldrich@gmail.com.
Gloria JalencasObstetrics and Gynecology Primary Care Center (ASSIR) Sabadell, Inst,tut Catala de la Salut, Barcelona, Spain.
Isabel MazanoObstetrics and Gynecology Primary Care Center (ASSIR) Sabadell, Inst,tut Catala de la Salut, Barcelona, Spain.
Cristina Lesmes-HerediaGynecology and Obstetrics Service, Parc Tauli University Hospital, Parc Taulí Research and Innovation Institute (I3PT-CERCA), Universitat Autònoma de Barcelona, Sabadell, Spain.
Josep-Maria Manresa-DominguezUnitat de Suport a la Recerca Metropolitana Nord, Fundació Institut Universitari per a la recerca a l'Atenció Primària de Salut Jordi Gol i Gurina (IDIAPJGol), Barcelona, Spain.
Maria Iniguez-CruzUnitat de Suport a la Recerca Metropolitana Nord, Fundació Institut Universitari per a la recerca a l'Atenció Primària de Salut Jordi Gol i Gurina (IDIAPJGol), Barcelona, Spain.
Joan-Carles FerreresPathological Anatomy Department, Parc Taulí University Hospital, Parc Taulí Research and Innovation Institute (I3PT-CERCA), Universitat Autònoma de Barcelona, Sabadell, Spain.
Viviana BeltranDiagnostic Imaging Service, Parc Tauli Health Corporation, Parc Taulí University Hospital, Parc Taulí Research and Innovation Institute (I3PT-CERCA), Universitat Autònoma de Barcelona, Sabadell, Spain.
Antoni BorrellFacultat de Medicina i Ciències de la Salut, Universitat de Barcelona (UB), Barcelona, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

<p>Introduction: The aim of this study was to assess the clinical utility of low-set ears (LSE) as a novel 2D-ultrasound marker for the prenatal detection of chromosomal anomalies.

methodsA multicenter cohort study including 1,331 singleton pregnancies between 11+2 and 34+6 weeks of gestation was conducted in the two participating centers to determine the performance of LSE as an aneuploidy marker. LSE was defined as a dichotomous marker using a newly defined axial plane of the fetal head in 2D ultrasound. Intra- and interobserver variability were assessed to ensure marker reliability. Efficacy in predicting chromosomal anomalies was assessed using LSE alone or in combination with aneuploidy screening.

resultsA new axial plane of the fetal head, defined by both lenses and the cerebellum, was adopted for LSE detection. Intra-observer concordance Kappa index for LSE measurement was 1.0, and 0.82 for interobserver reliability. LSE could be assessed in 99% of the studied fetuses and was detected in 30 (2.3%) fetuses: in 19 (86%) of the 22 fetuses with chromosomal anomalies, in all cases (5/5, 100%) with other genetic anomalies, and in six (18%) of the 34 malformed fetuses without a genetic disorder. In one (3.3%) of the fetuses, LSE was not confirmed postnatally while the remaining 29 fetuses had an adverse outcome. When LSE was combined with aneuploidy screening, the detection rate of chromosomal anomalies remained the same and specificity increased from 89% to 100%.

conclusionsOur study supports using LSE as a potential 2D-ultrasound marker for chromosomal anomaly detection. Studies with a larger sample size and in high-risk populations are warranted to prove its clinical utility before this marker can be included in prenatal screening protocols. </p>.

Indexed as

Chromosome AberrationsChromosome DisordersEarUltrasonography, PrenatalAneuploidyFemaleHumansPregnancyAneuploidyCohort studyFetal earFetal ultrasonographyLow-set ear

Identifiers

PMID41218004
PMCPMC12707868

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.