ArticleClinical case reports2025
A Rare Case of Antenatal Bilateral Multicystic Dysplastic Kidney Disease: An Unusual Presentation in a Neonate.
Article in Clinical case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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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.
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.
Who cites it
1 citing paper in PubMed.
- Paediatric multicystic dysplastic kidney disease in Cape Town, South Africa.BMC nephrology · 2025Article
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
This report highlights a deadly presentation of Multicystic dysplastic kidney (MCDK) diagnosed in utero and confirmed after 6 weeks post-delivery by ultrasonography. In this case, we present a neonate followed for a period of 6 weeks after delivery without any notable complications. From the literature point of view, this condition is incompatible with life and there are few cases reported in sub-Saharan Africa. There is no definitive treatment for such a case; only watchful waiting and serial renal function tests are used to monitor complications to date. Hence, this case opens a window for other researchers to evaluate this course, especially in resource-limited settings.
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Registered trials
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