Evidence map›Paper›PMID 41417372›Full record

ArticleRevista da Associacao Medica Brasileira (1992)2025

Prenatal diagnosis to postnatal outcomes in multicystic dysplastic kidney: experience of a tertiary center in the Black Sea region.

Gökhan Ünver, Sercan Serin, Miğraci Tosun, Handan Çelik, Mesut Önal, Ümmet Abur, Engin Altundağ

Abstract read
In one paragraph

Article in Revista da Associacao Medica Brasileira (1992), 2025. 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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1 · What the graph read from it

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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

7 authors.

Gökhan ÜnverOndokuz Mayis University, Faculty of Medicine, Department of Obstetrics and Gynecology, Perinatology Unit - Samsun, Turkey.ORCID http://orcid.org/0000-0002-0887-2634
Sercan SerinOndokuz Mayis University, Faculty of Medicine, Department of Obstetrics and Gynecology, Perinatology Unit - Samsun, Turkey.ORCID http://orcid.org/0000-0003-2477-138X
Miğraci TosunOndokuz Mayis University, Faculty of Medicine, Department of Obstetrics and Gynecology, Perinatology Unit - Samsun, Turkey.ORCID http://orcid.org/0000-0003-1548-5111
Handan ÇelikOndokuz Mayis University, Faculty of Medicine, Department of Obstetrics and Gynecology - Samsun, Turkey.ORCID http://orcid.org/0000-0001-5201-9385
Mesut ÖnalOndokuz Mayis University, Faculty of Medicine, Department of Obstetrics and Gynecology - Samsun, Turkey.ORCID http://orcid.org/0000-0003-1222-3386
Ümmet AburOndokuz Mayis University, Faculty of Medicine, Department of Medical Genetics - Samsun, Turkey.ORCID http://orcid.org/0000-0002-4811-9321
Engin AltundağOndokuz Mayis University, Faculty of Medicine, Department of Medical Genetics - Samsun, Turkey.ORCID http://orcid.org/0000-0001-8841-1426

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe aim of this study was to determine the association of unilateral multicystic dysplastic kidney in fetuses with genetic disorders, syndromic conditions, accompanying anatomical anomalies, and postnatal prognosis.

methodsCases diagnosed with multicystic dysplastic kidney and followed at the Perinatology Clinic of Samsun Ondokuz Mayıs University between January 2012 and June 2024 were retrospectively reviewed. Demographic, ultrasonographic, genetic, and postnatal outcomes were analyzed.

resultsThirty-eight fetuses with multicystic dysplastic kidney were identified during intrauterine life. The diagnosis was made via antenatal ultrasonography in 97.2% of cases. Laterality was on the left side in 55.3% and on the right side in 44.7% of multicystic dysplastic kidney cases. The cohort consisted of 42.1% females and 57.9% males. Major extrarenal anomalies were present in 21.1% of fetuses with unilateral multicystic dysplastic kidney. Amniocentesis for karyotyping was performed in 23.7% of cases, all of which yielded normal karyotypes. Contralateral kidney anomalies were detected in 13.2% of cases, and ureterocele was observed in 15.8%. The most common postnatal anomalies were ureteropelvic junction obstruction and grade four-five vesicoureteral reflux. During a mean follow-up period of 7 years, no cases of hypertension or Wilms tumor were identified.

conclusionPrenatal diagnosis of multicystic dysplastic kidney is crucial for early detection of potential contralateral kidney anomalies and predicting postnatal outcomes. In cases of isolated multicystic dysplastic kidney, the likelihood of karyotypic abnormalities, malignancies, or hypertension is very low, and the postnatal prognosis is favorable.

Indexed as

Multicystic Dysplastic KidneyUltrasonography, PrenatalAdultFemaleGestational AgeHumansInfant, NewbornMalePregnancyPrenatal DiagnosisPrognosisRetrospective StudiesTertiary Care CentersTurkey

Identifiers

PMID41417372
PMCPMC12711117

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