Literature DB >> 2149599

[Familial hyperkalemia syndrome (Gordon's syndrome)].

M Baz1, Y Berland, B Dussol, K Jaber, Y Boobes.   

Abstract

Hyperkaliema at 6 mmol/l was discovered in a 30-year old man during routine examination. Further investigations showed that the hyperkaliaemia was associated with hyperchloraemic acidosis, stimulable hyporeninaemia and relative hypoaldosteronism in relation to the hyperkaliaemia. Renal and adrenal functions were normal. The finding of 3 identical cases in a French family of 9 persons led to the diagnosis of Gordon's syndrome, a rare hereditary metabolic disorder with a controverted physiopathology.

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Year:  1990        PMID: 2149599

Source DB:  PubMed          Journal:  Presse Med        ISSN: 0755-4982            Impact factor:   1.228


  1 in total

1.  Disease-causing R1185C mutation of WNK4 disrupts a regulatory mechanism involving calmodulin binding and SGK1 phosphorylation sites.

Authors:  Tao Na; Guojin Wu; Wei Zhang; Wen-Ji Dong; Ji-Bin Peng
Journal:  Am J Physiol Renal Physiol       Date:  2012-10-10
  1 in total

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