Bartter syndrome laboratory findings: Difference between revisions

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Main Article: [[Bartter syndrome]]
 
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==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<ref name="pmid23345488">{{cite journal| author=Cruz AJ, Castro A| title=Gitelman or Bartter type 3 syndrome? A case of distal convoluted tubulopathy caused by CLCNKB gene mutation. | journal=BMJ Case Rep | year= 2013 | volume= 2013 | issue= | pages= | pmid=23345488 | doi=10.1136/bcr-2012-007929 | pmc=3604527 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23345488 }} </ref><ref name="pmid12506158">{{cite journal| author=Konrad M, Weber S| title=Recent advances in molecular genetics of hereditary magnesium-losing disorders. | journal=J Am Soc Nephrol | year= 2003 | volume= 14 | issue= 1 | pages= 249-60 | pmid=12506158 | doi=10.1097/01.asn.0000049161.60740.ce | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12506158 }} </ref>
 
==References==
==References==
{{Reflist|2}}
{{Reflist|2}}
[[Category:Needs content]]


[[Category:Disease]]
[[Category:Disease]]

Latest revision as of 20:37, 5 August 2020

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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

References

  1. 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.
  2. 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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