Evidence map›Paper›PMID 41595474›Full record

ArticleGenes2026

Prenatal Diagnosis of a Feingold Syndrome Pregnancy Complicated with Severe Preeclampsia: A Report of a Challenging Case.

Athina A Samara, Paraskevas Perros, Antonios Koutras, Michel B Janho, Emmanuil Manolakos, Nikoletta Daponte, Apostolos C Ziogas, Antonios Garas, Chara Skentou, Sotirios Sotiriou

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PubMed Full text at PMC Publisher
In one paragraph

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

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

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Athina A SamaraDepartment of Embryology, Faculty of Medicine, University of Thessaly, Mezourlo, 41110 Larissa, Greece.ORCID 0000-0002-6177-7281
Paraskevas PerrosDepartment of Obstetrics and Gynecology, Alexandra Maternity Hospital of Athens, National Kapodistrian University of Athens, Lourou 4, 11528 Athens, Greece.ORCID 0009-0000-6454-7855
Antonios KoutrasDepartment of Obstetrics and Gynecology, Alexandra Maternity Hospital of Athens, National Kapodistrian University of Athens, Lourou 4, 11528 Athens, Greece.ORCID 0000-0002-7229-9983
Michel B JanhoDepartment of Obstetrics and Gynecology, Faculty of Medicine, University of Thessaly, Mezourlo, 41110 Larissa, Greece.ORCID 0000-0003-1776-0009
Emmanuil ManolakosAccess to Genome, Michalacopoulou 139, 11528 Athens, Greece.
Nikoletta DaponteDepartment of Obstetrics and Gynecology, Faculty of Medicine, University of Thessaly, Mezourlo, 41110 Larissa, Greece.
Apostolos C ZiogasDepartment of Obstetrics and Gynecology, Faculty of Medicine, University of Thessaly, Mezourlo, 41110 Larissa, Greece.ORCID 0000-0002-3377-6935
Antonios GarasDepartment of Obstetrics and Gynecology, Faculty of Medicine, University of Thessaly, Mezourlo, 41110 Larissa, Greece.
Chara SkentouDepartment of Obstetrics and Gynecology, Faculty of Medicine, University of Ioannina, S. Niarhou, 45500 Ioannina, Greece.
Sotirios SotiriouDepartment of Embryology, Faculty of Medicine, University of Thessaly, Mezourlo, 41110 Larissa, Greece.ORCID 0000-0002-9466-6086

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Feingold syndrome (FS) is a rare congenital disorder with an autosomal dominant inheritance pattern. Two distinct subtypes are recognized based on their molecular pathology: FS type 1 (FS1) and FS type 2 (FS2). Both types share skeletal anomalies such as microcephaly, brachymesophalangia, and clinodactyly; however, gastrointestinal atresia is unique to FS1. Herein, we report a rare prenatal diagnosis of FS1 in a female fetus. The second-trimester ultrasound revealed bilateral clinodactyly and fetal microcephaly, and the subsequent molecular karyotyping identified a ~342 kb deletion at 2p24.3 encompassing the

Indexed as

Intellectual DisabilityLimb Deformities, CongenitalMicrocephalyPre-EclampsiaPrenatal DiagnosisAdultEyelidsFemaleHumansInfant, NewbornN-Myc Proto-Oncogene ProteinPregnancyTracheoesophageal FistulaUltrasonography, PrenatalN-Myc Proto-Oncogene Proteinbilateral clinodactylyFeingold syndromegastrointestinal disordersintellectual impairmentmicrocephalyshort stature

Identifiers

PMID41595474
PMCPMC12840743

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Registered trials

None linked

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.