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Results 1 - 9 of 9 for Calcium chloride
  1. Gnathodiaphyseal dysplasia 
    ... atoms (calcium ions); these channels are known as calcium-activated chloride channels. The mechanism for this calcium activation is unclear.The ANO5 gene mutations that ...
    https://medlineplus.gov/.../condition/gnathodiaphyseal-dysplasia - Genetics
  2. Bartter syndrome 
    ... thrive). They lose excess amounts of salt (sodium chloride) in their urine, which leads to dehydration, constipation, and increased urine production (polyuria). In addition, large amounts of calcium are lost through the urine (hypercalciuria), which can ...
    https://medlineplus.gov/genetics/condition/bartter-syndrome - Genetics
  3. Episodic ataxia 
    ... the protein produced from the CACNA1A gene transports calcium ions. The ... transports chloride ions across cell membranes. The movement of chloride ...
    https://medlineplus.gov/genetics/condition/episodic-ataxia - Genetics
  4. Pseudohypoaldosteronism type 2 
    ... life. Affected individuals also have high levels of chloride (hyperchloremia) and acid ... PHA2 is a rare ...
    https://medlineplus.gov/.../condition/pseudohypoaldosteronism-type-2 - Genetics
  5. Gitelman syndrome 
    ... involved in the kidneys' reabsorption of salt (sodium chloride or NaCl) from ... magnesium, and calcium. The resulting imbalance of ions in the body ...
    https://medlineplus.gov/genetics/condition/gitelman-syndrome - Genetics
  6. Childhood absence epilepsy 
    ... a channel that allows negatively charged chlorine atoms (chloride ions) to cross the cell membrane. The influx of chloride ions in nerve cells (neurons) in developed brains ...
    https://medlineplus.gov/.../condition/childhood-absence-epilepsy - Genetics
  7. Juvenile myoclonic epilepsy 
    ... a channel that allows negatively charged chlorine atoms (chloride ions) to cross the cell membrane. After infancy, the influx of chloride ions creates an environment in the cell that ...
    https://medlineplus.gov/.../condition/juvenile-myoclonic-epilepsy - Genetics
  8. Dent disease 
    ... on PubMed Central Devuyst O. Dent's disease: chloride-proton exchange controls proximal tubule endocytosis. Nephrol Dial ... O, Jentsch TJ, Thakker RV. Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) ...
    https://medlineplus.gov/genetics/condition/dent-disease - Genetics
  9. SLC4A1-associated distal renal tubular acidosis 
    ... Specifically, AE1 exchanges negatively charged atoms of chlorine (chloride ions) for negatively charged bicarbonate molecules (bicarbonate ions). ...
    https://medlineplus.gov/...-associated-distal-renal-tubular-acidosis - Genetics