Evidence map›Paper›PMID 41749627›Full record

ArticleChildren (Basel, Switzerland)2026

Trisomy 18 and Trisomy 13: A Retrospective Cohort Study at a Tertiary Hospital.

Nihan Uygur Külcü, Nurdan Erol, Sümeyra Oguz, Ayşenur Celayir, Güner Karatekin, Özge Yatır Alkan

Abstract read
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Article in Children (Basel, Switzerland), 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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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Nihan Uygur KülcüDepartment of Pediatrics, University of Health Sciences, Zeynep Kamil Maternity and Children's Training and Research Hospital, 34668 Istanbul, Türkiye.ORCID 0000-0001-8771-5292
Nurdan ErolDepartment of Pediatrics, University of Health Sciences, Zeynep Kamil Maternity and Children's Training and Research Hospital, 34668 Istanbul, Türkiye.ORCID 0000-0002-9650-2077
Sümeyra OguzDepartment of Medical Genetics, University of Health Sciences, Zeynep Kamil Maternity and Children's Training and Research Hospital, 34668 Istanbul, Türkiye.ORCID 0000-0003-4001-0505
Ayşenur CelayirDepartment of Pediatric Surgery, University of Health Sciences, Zeynep Kamil Maternity and Children's Training and Research Hospital, 34668 Istanbul, Türkiye.ORCID 0000-0002-7809-4137
Güner KaratekinDepartment of Neonatology, University of Health Sciences, Zeynep Kamil Maternity and Children's Training and Research Hospital, 34668 Istanbul, Türkiye.ORCID 0000-0001-7112-0323
Özge Yatır AlkanDepartment of Neonatology, University of Health Sciences, Zeynep Kamil Maternity and Children's Training and Research Hospital, 34668 Istanbul, Türkiye.ORCID 0000-0002-4323-4224

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTrisomy 18 (T18; Edwards syndrome) and Trisomy 13 (T13; Patau syndrome) are rare autosomal aneuploidies characterized by severe congenital anomalies, high neonatal mortality, and complex clinical trajectories.

objectiveThis study aimed to describe the clinical features, management approaches, and outcomes of genetically confirmed patients aged 0-18 years diagnosed with T18 or T13 in a tertiary care center.

methodsThis retrospective study reviewed hospital records of genetically confirmed T18 and T13 cases identified through ICD-10 codes (Q91-Q92) between January 2015 and December 2024. Patients aged 0-18 years at diagnosis were included. Demographic, clinical, and interventional data were collected from electronic medical records. Survival analyses were conducted using the Kaplan-Meier method, with comparisons assessed using the log-rank test.

resultsAmong 29 patients, 23 had T18 and 6 had T13. Cardiovascular involvement was the most frequent anomaly, and overall mortality was high despite intensive care. Median survival was 90 days for T18 and 120 days for T13, with more than 80% surviving the first month but showing a steep decline thereafter. Most deaths were attributed to cardiopulmonary complications or sepsis secondary to prolonged intensive care. Kaplan-Meier analysis revealed marked early mortality in both groups, with no significant survival difference (log-rank

conclusionsT18 and T13 are associated with high early mortality driven by complex congenital heart disease, respiratory instability, and infection-related complications. Although the overall prognosis remains poor, a minority of patients achieve extended survival, highlighting variable trajectories. Early multidisciplinary care, individualized decision-making, and strict infection prevention remain essential to optimize outcomes and support families.

Indexed as

congenital heart diseaseintensive care unitKaplan–Meier curveneonatal mortalitynosocomial infectionsurvival analysisTrisomy 13Trisomy 18

Identifiers

PMID41749627
PMCPMC12939952

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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.