Hypocalciuria

Common Name(s)

Hypocalciuria

Description for this condition is not yet available.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Hypocalciuria" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Hypocalciuria" returned 3 free, full-text research articles on human participants. First 3 results:

Enhanced passive Ca2+ reabsorption and reduced Mg2+ channel abundance explains thiazide-induced hypocalciuria and hypomagnesemia.
 

Author(s): Tom Nijenhuis, Volker Vallon, Annemiete W C M van der Kemp, Johannes Loffing, Joost G J Hoenderop, René J M Bindels

Journal: J. Clin. Invest.. 2005 Jun;115(6):1651-8.

 

Thiazide diuretics enhance renal Na+ excretion by blocking the Na+-Cl- cotransporter (NCC), and mutations in NCC result in Gitelman syndrome. The mechanisms underlying the accompanying hypocalciuria and hypomagnesemia remain debated. Here, we show that enhanced passive Ca2+ transport ...

Last Updated: 31 Dec 1969

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Renal potassium wasting and hypocalciuria ameliorated with magnesium repletion in Gitelman's syndrome.
 

Author(s): Y J Cho, G T Park, Y J Cho, H J Kim

Journal: J. Korean Med. Sci.. 1997 Apr;12(2):157-9.

 

A woman aged 45 years was presented with hypokalemic metabolic alkalosis and hypomagnesemia associated with renal potassium and magnesium wasting. Her 24-hour urinary calcium excretion was strikingly low despite normocalcemia and normal creatinine clearance, which is one of characteristic ...

Last Updated: 31 Dec 1969

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Urinary calcium excretion in familial hypocalciuric hypercalcemia. Persistence of relative hypocalciuria after induction of hypoparathyroidism.
 

Author(s): M F Attie, J R Gill, J L Stock, A M Spiegel, R W Downs, M A Levine, S J Marx

Journal: J. Clin. Invest.. 1983 Aug;72(2):667-76.

 

Familial hypocalciuric hypercalcemia (FHH) is an autosomal dominant trait comprising hypercalcemia, hypophosphatemia, parathyroid hyperplasia, and unusually low renal clearance of calcium. We evaluated the role of parathyroid hormone in the relative hypocalciuria of FHH and characterized ...

Last Updated: 31 Dec 1969

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Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Hypocalciuria" returned 0 free, full-text review articles on human participants.

 
 
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Symptoms, Diagnosis, and Treatment

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Clinical Trial Information This information is provided by ClinicalTrials.gov

There are currently no open clinical trials for this condition.