Bartter syndrome laboratory findings
Main Article: Bartter syndrome
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Tayyaba Ali, M.D.[2]
Overview
Laboratory findings such as Hypokalemia, Metabolic alkalosis, Elevated plasma renin and aldosterone, Elevated urine potassiun and chloride, Low serum and urine magnesium levels.
Laboratory Findings
- Hypokalemia
- Metabolic alkalosis
- Elevated plasma renin and aldosterone
- Elevated urine potassiun and chloride
- Low serum and urine magnesium levels[1][2]
References
- ↑ Cruz AJ, Castro A (2013). “Gitelman or Bartter type 3 syndrome? A case of distal convoluted tubulopathy caused by CLCNKB gene mutation”. BMJ Case Rep. 2013. doi:10.1136/bcr-2012-007929. PMC 3604527. PMID 23345488.
- ↑ Konrad M, Weber S (2003). “Recent advances in molecular genetics of hereditary magnesium-losing disorders”. J Am Soc Nephrol. 14 (1): 249–60. doi:10.1097/01.asn.0000049161.60740.ce. PMID 12506158.
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