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Published in: Journal of Medical Case Reports 1/2009

Open Access 01-12-2009 | Case report

Medullary sponge kidney presenting in a neonate with distal renal tubular acidosis and failure to thrive: a case report

Authors: Mohamed El-Sawi, Abdul-Rahman Shahein

Published in: Journal of Medical Case Reports | Issue 1/2009

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Abstract

Introduction

Medullary sponge kidney is a congenital anomaly characterized by diffuse ectasy of the collecting tubules of one or both kidneys. It is usually diagnosed in the second or third decade of life.

Case presentation

Distal renal tubular acidosis is commonly observed in patients with medullary sponge kidney. We describe here a 50-day-old Egyptian Caucasian girl with medullary sponge kidney who had features of distal renal tubular acidosis, (persistent alkaline urine, hypercalciuria, hypocitraturia) and failure to thrive. Renal ultrasound revealed left renal increased medullary echogenicity and bilateral nephrocalcinosis.

Conclusion

Early gene(s) expression of medullary sponge kidney disease might be responsible for persistent metabolic acidosis during the neonatal period.
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Metadata
Title
Medullary sponge kidney presenting in a neonate with distal renal tubular acidosis and failure to thrive: a case report
Authors
Mohamed El-Sawi
Abdul-Rahman Shahein
Publication date
01-12-2009
Publisher
BioMed Central
Published in
Journal of Medical Case Reports / Issue 1/2009
Electronic ISSN: 1752-1947
DOI
https://doi.org/10.1186/1752-1947-3-6656

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