Rapidly progressive nephromegaly in a neonate with autosomal recessive poly cystic kidney disease
Background: Autosomal recessive polycystic kidney disease (ARPKD) associates with significant renal and liver-related morbidity and mortality in children. Rarely severe enlargement of kidneys necessitates nephrectomy and initiating dialysis. Case Presentation: A 5-day-old newborn boy with prenatal u...
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| Main Authors: | , , , |
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| Format: | Book |
| Published: |
Society of Diabetic Nephropathy Prevention,
2017-10-01T00:00:00Z.
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Connect to this object online.3rd Floor Main Library
| Call Number: |
A1234.567 |
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| Copy 1 | Available |