Abstract
This article provides an up-to-date comprehensive review and summary on neonatal polycystic kidney disease (PKD) with emphasis on the differential diagnosis, clinical manifestations, diagnostic techniques, and potential therapeutic approaches for the major causes of neonatal PKD, namely hereditary disease, including autosomal recessive and autosomal dominant PKD and nonhereditary PKD, with particular emphasis on multicystic dysplastic kidney. A brief overview of obstructive cystic dysplasia and simple and complex cysts is also included.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 543-560 |
| Number of pages | 18 |
| Journal | Clinics in Perinatology |
| Volume | 41 |
| Issue number | 3 |
| DOIs | |
| State | Published - Sep 2014 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- ADPKD
- ARPKD
- Multicystic dysplastic kidney
- Polycystic kidney
- Renal cyst
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