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Gitelman Syndrome  

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Tipo

  • mesh:Descriptor

Definición

  • 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.

Etiquetas alternativas

  • 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

En otras lenguas

URI

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

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