A Novel Homozygous Mutation of Classic Bartter Syndrome Presenting with Renal Cysts in 6-year-Old Identical Twin Boys : A Case Report
Bartter syndrome is an autosomal recessive hypokalemic salt-losing tubulopathy, and classic Bartter syndrome is associated with mutations in the CLCNKB gene. While chronic hypokalemia is known to induce renal cyst formation in different renal diseases, renal cyst formation in Bartter syndrome is rar...
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| Main Authors: | , , |
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| Format: | Book |
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Korean Society of Pediatric Nephrology,
2021-06-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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