Evidence map›Paper›PMID 40040326›Full record

ArticleActa obstetricia et gynecologica Scandinavica2025

Sonographic diagnosis of fetal eye anomalies and their association with syndromal diseases: A retrospective multicenter analysis of 264 cases.

Jorge Jiménez Cruz, Paul Böckenhoff, Laura Tascón Padrón, Norah Emrich, Philipp Kosian, Brigitte Strizek, Cristoph Berg, Eva Weber, Ulrich Gembruch, Annegret Geipel

Abstract readMulticenter Study
In one paragraph

Article in Acta obstetricia et gynecologica Scandinavica, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Jorge Jiménez CruzDepartment of Obstetrics and Prenatal Medicine, Bonn University Hospital, Bonn, Germany.ORCID 0000-0002-1892-790X
Paul BöckenhoffDepartment of Obstetrics and Prenatal Medicine, Bonn University Hospital, Bonn, Germany.ORCID 0000-0001-7875-832X
Laura Tascón PadrónDepartment of Obstetrics and Prenatal Medicine, Bonn University Hospital, Bonn, Germany.ORCID 0000-0001-9941-9001
Norah EmrichDepartment of Obstetrics and Prenatal Medicine, Bonn University Hospital, Bonn, Germany.ORCID 0000-0003-1705-1536
Philipp KosianDepartment of Obstetrics and Prenatal Medicine, Bonn University Hospital, Bonn, Germany.
Brigitte StrizekDepartment of Obstetrics and Prenatal Medicine, Bonn University Hospital, Bonn, Germany.ORCID 0000-0003-3625-7097
Cristoph BergDepartment of Obstetrics and Prenatal Medicine, Bonn University Hospital, Bonn, Germany.
Eva WeberDepartment of Obstetrics and Prenatal Medicine, Cologne University Hospital, Cologne, Germany.
Ulrich GembruchDepartment of Obstetrics and Prenatal Medicine, Bonn University Hospital, Bonn, Germany.
Annegret GeipelDepartment of Obstetrics and Prenatal Medicine, Bonn University Hospital, Bonn, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThis study aims to systematically describe eye malformations and correlate these with extraocular findings. Based on these findings, we propose a protocol for ultrasound evaluation of the fetal eye. MATERIAL AND

methodsIn this multicentric retrospective cohort study, 264 fetuses with ocular malformations from two tertiary referral centers for prenatal medicine were analyzed. Anophthalmia, microphthalmia, exophthalmos, hyper- or hypotelorism, cataract, aphakia, cyclopia, and retinal detachment were assessed, and their association with extraocular findings and genetic changes was investigated.

resultsThe majority of the cases (99.2%) were non-isolated and presented further extraocular findings. Most commonly, the brain and central nervous system (65.9%), the limbs and the heart (46.6% each) and the cranial anatomy (41.2%) were affected. Significant associations were found between exophthalmos and anomalies of the fetal skeletal system (OR = 4.8, 95% CI 1.6-14) and cranial malformations (OR = 3.3, 95% CI 1.5-7.4). Hypotelorism showed an increased risk of cardiac anomalies (OR = 1.8, 95% CI 1.1-3.5) and brain malformations (OR = 2.16, 95% CI 1.2-4.1), with holoprosencephaly being the most common one. Fetuses with microphthalmia were more likely to have anomalies in the renal system (OR = 2.3, 95% CI 1.2-4.3). In 51.4% of the cases, a genetic aberration could be found, among them most frequently trisomy 13.

conclusionsThere is a significant association between specific fetal eye anomalies and certain extraocular anomalies, as well as genetic changes. Systematic evaluation of the eye using the proposed protocol is simple to learn and highly reproducible and could help to concentrate diagnosis on a certain group of malformations. Data from this study could help to develop targeted diagnostic molecular tools.

Indexed as

Abnormalities, MultipleEye AbnormalitiesUltrasonography, PrenatalAdultFemaleHumansPregnancyRetrospective StudiesSyndromefetal eyefetal syndromesfetal ultrasoundocular malformationsorbital malformations

Identifiers

PMID40040326
PMCPMC11981110

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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.