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Results 1 - 5 of 5 for Familial "hypokalemia-hypomagnesemia"
  1. Gitelman syndrome 
    ... not show signs and symptoms of the condition. Familial hypokalemia-hypomagnesemia Gitelman's syndrome GS Hypokalemia-hypomagnesemia, primary renotubular, ...
    https://medlineplus.gov/genetics/condition/gitelman-syndrome - Genetics
  2. Bartter syndrome 
    Bartter syndrome is a group of very similar kidney disorders that cause an imbalance of potassium, sodium, chloride, and related molecules in the body.In some ...
    https://medlineplus.gov/genetics/condition/bartter-syndrome - Genetics
  3. SLC12A3 gene 
    ... SLC12A3 gene have been identified in people with Gitelman syndrome. Most of these mutations change single protein building ... in the body underlies the major features of Gitelman syndrome. More About This Health Condition Some research suggests ...
    https://medlineplus.gov/genetics/gene/slc12a3 - Genetics
  4. CLCNKB gene 
    ... the CLCNKB gene are a rare cause of Gitelman syndrome. Like the mutations responsible for Bartter syndrome, the genetic changes associated with Gitelman syndrome impair the kidneys' ability to reabsorb salt, leading ...
    https://medlineplus.gov/genetics/gene/clcnkb - Genetics
  5. Kidney Diseases (National Library of Medicine)  
    You have two kidneys, each about the size of your fist. They are near the middle of your back, just below the rib cage. Inside each kidney there are about ...
    https://medlineplus.gov/kidneydiseases.html - Health Topics