Management of childhood Gitelman syndrome: a case study
Gitelman syndrome is a rare, autosomal recessive, renal tubular salt wasting disorder characterized by hypokalemia, and metabolic alkalosis in combination with significant hypomagnesemia and hypocalciuria.1,2 The prevalence is estimated to be 1 in 40,000 individuals. The condition affects both males...
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Format: | Book |
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Indonesian Pediatric Society Publishing House,
2016-07-01T00:00:00Z.
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A1234.567 |
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