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Results 1 - 10 of 19 for Hypokalemic alkalosis
  1. 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
  2. Bartter syndrome 
    ... an abnormal acid balance in the blood called hypokalemic alkalosis, which causes too much calcium in the urine. ... Bartter syndrome is usually suspected when a blood test finds a low level of potassium in the blood . ...
    https://medlineplus.gov/ency/article/000308.htm - Medical Encyclopedia
  3. Aldosterone blood test 
    ... normal level of aldosterone may be due to: Bartter syndrome (group of rare conditions that affect the kidneys) ...
    https://medlineplus.gov/ency/article/003704.htm - Medical Encyclopedia
  4. SLC12A1 gene 
    ... SLC12A1 gene have been identified in people with Bartter syndrome type I. This form of the disorder is ... Most of the SLC12A1 gene mutations responsible for Bartter syndrome change single protein building blocks (amino acids) in ...
    https://medlineplus.gov/genetics/gene/slc12a1 - Genetics
  5. Alkalosis 
    ... loss of chloride, such as from prolonged vomiting. Hypokalemic alkalosis is caused by the kidneys' response to an ...
    https://medlineplus.gov/ency/article/001183.htm - Medical Encyclopedia
  6. Gitelman syndrome 
    Gitelman syndrome is a kidney disorder that causes an imbalance of charged atoms (ions) in the body, including ions of potassium, magnesium, and calcium.The signs ...
    https://medlineplus.gov/genetics/condition/gitelman-syndrome - Genetics
  7. BSND gene 
    ... BSND gene have been identified in people with Bartter syndrome type IV. This form of the disorder causes ... abnormalities in the inner ear, which is why Bartter syndrome type IV is also known as antenatal Bartter ...
    https://medlineplus.gov/genetics/gene/bsnd - Genetics
  8. CLCNKB gene 
    ... CLCNKB gene have been identified in people with Bartter syndrome type III. This form of the condition, which is also described as classical Bartter syndrome, begins in childhood and tends to be less ...
    https://medlineplus.gov/genetics/gene/clcnkb - Genetics
  9. CLCNKA gene 
    ... a role in normal hearing. Several people with Bartter syndrome have had mutations in both the CLCNKA gene ... a life-threatening form of the disorder called Bartter syndrome type IV. This condition is also known as ...
    https://medlineplus.gov/genetics/gene/clcnka - Genetics
  10. KCNJ1 gene 
    ... KCNJ1 gene have been identified in people with Bartter syndrome type II. This form of the disorder causes ... Some of the KCNJ1 gene mutations responsible for Bartter syndrome change single protein building blocks (amino acids) in ...
    https://medlineplus.gov/genetics/gene/kcnj1 - Genetics
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