Evidence map›Paper›PMID 40130570›Full record

ReviewArchives of endocrinology and metabolism2025

Placental insufficiency irrespective of offspring karyotype in maternal Turner syndrome: a case series and literature review.

Beáta Vida, Olga Török, Zoárd Tibor Krasznai, Zsuzsanna Buczkó, Péter Juhász, Gábor Méhes, Mónika Orosz, Attila Jakab, Tamás Deli

Abstract readReviewCase Reports
In one paragraph

Review in Archives of endocrinology and metabolism, 2025. 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

9 authors.

Beáta VidaDepartment of Obstetrics and Gynaecology, University of Debrecen, Debrecen, Hungary.ORCID 0000-0002-0636-8514
Olga TörökDepartment of Obstetrics and Gynaecology, University of Debrecen, Debrecen, Hungary.ORCID 0009-0001-8379-3872
Zoárd Tibor KrasznaiDepartment of Obstetrics and Gynaecology, University of Debrecen, Debrecen, Hungary.ORCID 0000-0003-2149-3935
Zsuzsanna BuczkóDepartment of Obstetrics and Gynaecology, University of Debrecen, Debrecen, Hungary.ORCID 0009-0001-1203-908X
Péter JuhászDepartment of Pathology, University of Debrecen, Debrecen, Hungary.ORCID 0000-0002-9102-6577
Gábor MéhesDepartment of Pathology, University of Debrecen, Debrecen, Hungary.ORCID 0000-0003-2503-7451
Mónika OroszDepartment of Obstetrics and Gynaecology, University of Debrecen, Debrecen, Hungary.ORCID 0009-0004-9049-5699
Attila JakabDepartment of Obstetrics and Gynaecology, University of Debrecen, Debrecen, Hungary.ORCID 0000-0002-2266-2297
Tamás DeliDepartment of Obstetrics and Gynaecology, University of Debrecen, Debrecen, Hungary.ORCID 0000-0003-2980-1656

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Turner syndrome is one of the most common aneuploidies. In vitro fertilization with oocyte donation is the usual method of assisted conception, but spontaneous pregnancy can also occur. Although pregnancies in Turner syndrome are widely accepted to be associated with small for gestational age foetuses, neither the causal role of placental insufficiency nor the contribution of maternal and foetal factors is well understood. Between 2009 and 2023, we followed 75 patients diagnosed with Turner syndrome at our university clinic, and four Turner syndrome patients became pregnant (4/75; 5.3%): ten pregnancies with seven live births (7/10; 70%) were reported. Conception was spontaneous in 6/7 patients (86%), and one patient had in vitro fertilization with oocyte donation. Two Turner syndrome patients with karyotype 45,X and two Turner syndrome patients with mosaicism (45,X/46,XX) were identified. Prenatal transabdominal amniocentesis revealed aneuploidy (45,X) in two foetuses. The most common obstetric complication was placental insufficiency, which presented as intrauterine growth restriction and foetal distress. Four early-term deliveries, one late-term delivery, one preterm delivery, and one extremely premature delivery occurred, and all pregnancies were terminated by caesarean section. No severe maternal complications during pregnancy were reported. Only newborns with Turner syndrome had long-term health problems. In Turner syndrome patients, even if pregnancy is conceived spontaneously, no maternal complications occur, and the foetus also has a normal karyotype, there is still a high prevalence of placental insufficiency and foetal compromise. The presented cases highlight the possible role of inherent maternal factors in Turner syndrome-associated intrauterine growth restriction and emphasize the importance of enhanced obstetric surveillance even in apparently uncomplicated Turner syndrome pregnancies.

Indexed as

Placental InsufficiencyPregnancy ComplicationsTurner SyndromeAdultFemaleFetal Growth RetardationHumansInfant, NewbornKaryotypeKaryotypingMosaicismPregnancyPregnancy Outcome

Identifiers

PMID40130570
PMCPMC11932634

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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.