A Rare Case of Antenatal Bilateral Multicystic Dysplastic Kidney Disease: An Unusual Presentation in a Neonate
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.
Authors
- Shaffin Rajan
- Hilary Chipongo (ORCID: https://orcid.org/0000-0002-1184-7077)
- Ronald Mclarty (ORCID: https://orcid.org/0000-0002-5459-9659)
- Samina Chaki
- Isack Mzolo
Institutions
- Aga Khan Hospital Dar es Salaam (TZ)
Publication Details
- Journal
- Clinical Case Reports
- Published
- 2025-04-01
- DOI
- https://doi.org/10.1002/ccr3.70407
- Citations
- 2
- Primary Topic
- Pediatric Urology and Nephrology Studies
- Type
- article
- Field-Weighted Citation Impact
- 6.99