Bartter syndrome laboratory findings: Difference between revisions
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__NOTOC__ | __NOTOC__ | ||
{{Bartter syndrome}} | {{Bartter syndrome}} | ||
Main Article: [[Bartter syndrome]] | |||
{{CMG}}{{AE}}{{TAM}} | {{CMG}}{{AE}}{{TAM}} | ||
==Overview== | ==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== | ==Laboratory Findings== | ||
*[[Hypokalemia]] | *[[Hypokalemia]] | ||
| Line 8: | Line 11: | ||
*Elevated plasma [[renin]] and [[aldosterone]] | *Elevated plasma [[renin]] and [[aldosterone]] | ||
*Elevated urine potassiun and chloride | *Elevated urine potassiun and chloride | ||
*Low serum and urine [[magnesium]]<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> | *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== | ||
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
- 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.