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Concept information

Terme préférentiel

Gitelman Syndrome  

Type

  • mesh:Descriptor

Définition

  • An inherited renal disorder characterized by defective NaCl reabsorption in the convoluted DISTAL KIDNEY TUBULE leading to HYPOKALEMIA. In contrast with BARTTER SYNDROME, Gitelman syndrome includes hypomagnesemia and normocalcemic hypocalciuria, and is caused by mutations in the thiazide-sensitive SODIUM-POTASSIUM-CHLORIDE SYMPORTERS.

Synonyme(s)

  • Familial Hypokalemia-Hypomagnesemia
  • Gitelman's Syndrome
  • Hypokalemia-Hypomagnesemia, Primary Renotubular, with Hypocalciuria
  • Hypomagnesemia-Hypokalemia, Primary Renotubular, with Hypocalciuria
  • Potassium and Magnesium Depletion
  • Primary Renotubular, Hypokalemia-Hypomagnesemia with Hypocalciuria
  • Primary Renotubular, Hypomagnesemia-Hypokalemia with Hypocalciuria
  • Tubular Hypomagnesemia-Hypokalemia with Hypocalcuria

Traductions

URI

http://data.loterre.fr/ark:/67375/JVR-G0F3BGC7-2

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RDF/XML TURTLE JSON-LD Date de création 05/07/2006, dernière modification le 30/06/2021