Two Children Admitted With Hypokalemia: Familial Gitelman Syndrome

ALİ KARAGÖZ, HARUN PERU, ŞEVKET ARSLAN, İBRAHİM GÜNEY, LÜTFULLAH ALTINTEPE

  • Year : 2013
  • Vol : 29
  • Issue : 1
  •  Page : 39-41
Gitelman syndrome (GS) is an autosomal recessive renal tubuler disorder. This syndrome also referred to as familial hypokalemiahypomagnesemia. The prevalence is estimated at approximately 1/40000 and it cannot be diagnosed until adulthood. GS, is caused by inactivating mutations in the thiazide-sensitive sodiumchloride cotransporter in the distal convoluted tubule of kidney and is associated low urinary calcium excretion, hypomagnesemia. Mutations, also lead to disruption NaCl reabsorbsion and hypovolemia. Therefore hypokalemia and metabolic alkalosis occur with activated the renin angiotensin aldosterone system. The most common cause of hypokalemia is renal potassium loss. Herein, we report cases of two (brother) GS, characterized by renal loss of potassium.
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Description : None of the authors, any product mentioned in this article, does not have a material interest in the device or drug. Research, not supported by any external organization. grant full access to the primary data and, if requested by the magazine they agree to allow the examination of data.
Two Children Admitted With Hypokalemia: Familial Gitelman Syndrome
, Vol. 29 (1)
Received : 07.07.2011, Accepted : 07.07.2011, Published Online : 13.08.2018
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ISSN:1017-6616;
E-ISSN:2149-8059;