Evidence map›Paper›PMID 40057705›Full record

ArticleBMC pregnancy and childbirth2025

How should antenatal counseling be given to parents in the fetal corpus callosum agenesis?

Hasan Süt, Gülşah Aynaoğlu Yıldız

Abstract read
In one paragraph

Article in BMC pregnancy and childbirth, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Hasan SütDepartment of Obstetrics and Gynaecology, Ankara University Faculty of Medicine, Mamak, Ankara, RI, 06590, Turkey. hassann0@gmail.com.ORCID http://orcid.org/0000-0003-0982-3356
Gülşah Aynaoğlu YıldızDepartment of Obstetrics and Gynaecology, Ankara University Faculty of Medicine, Mamak, Ankara, RI, 06590, Turkey.ORCID http://orcid.org/0000-0002-3283-7783

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe aimed to review the corpus callosum agenesis (CCA) cases diagnosed and managed in our University to contribute to the literature about this antenatally diagnosed fetal cranial anomaly by revealing the antenatal and postnatal outcomes of CCA.

methodsThis retrospective and cross-sectional study examined CCA detected in our clinic between 2012 and 2021. Genetic results, accompanying additional anomalies, termination, and perinatal mortality rates were also calculated. Neurodevelopmental outcomes were revealed by investigating motor development, cognitive development, behavioral disorder, speech delay, personal-social backwardness, and epilepsy in cases of isolated CCA and non-isolated CCA in the postnatal period.

resultsData from 30 fetuses were evaluated during the study. The number of isolated CCA and non-isolated CCA cases is 11 (37.5%) and 19 (62.5%), respectively, and the number of partial CCA and complete CCA cases is 8 (26%) and 22 (74%), respectively. Among the 30 fetuses, the numbers of live births, chromosomal anomalies, perinatal mortalities, and terminations were found to be 14 (47%), 3 (10%), 3 (10%), and 13 (43%), respectively. Postnatal evaluation was performed in 14 children, and normal neurodevelopmental outcomes were observed in 5 (35.7%). All these children were from the isolated CCA group. Additionally, poor neurodevelopmental outcome was detected in 37.5% of isolated CCA.

conclusionIf CCA is detected in the fetus, additional ultrasonographic anomaly and genetic examination should be performed to differentiate isolated CCA from non-isolated CCA. While the termination option can be offered to the family by informing them about poor pregnancy outcomes in non-isolated CCA, counseling in isolated CCA remains contradictory, and more comprehensive prospective studies are needed.

trial registrationThis study was retrospectively registered and authorized by the local Ethics Committee of Ankara University (clinical trial date 06.06.2024/ number 1391402).

Indexed as

Agenesis of Corpus CallosumCounselingGenetic CounselingParentsAdultCross-Sectional StudiesFemaleHumansInfant, NewbornMalePregnancyPrenatal DiagnosisRetrospective StudiesUltrasonography, PrenatalAgenesis of corpus callosumCounselingNeurodevelopmentOutcomePrenatal diagnosis

Identifiers

PMID40057705
PMCPMC11889785

What Socratic holds

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LicenceCC BY-NC-ND
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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 Socratic graph.