Gitelman syndrome associated with chondrocalcinosis and severe neuropathy: a novel heterozygous mutation in SLC12A3 gene. [electronic resource]
Producer: 20210323Description: 67-70 p. digitalISSN:- 0048-7449
- Aged
- Chondrocalcinosis -- complications
- Electromyography
- Furosemide -- administration & dosage
- Gitelman Syndrome -- complications
- Glycyrrhiza -- adverse effects
- Humans
- Hypercalciuria -- complications
- Male
- Nephrocalcinosis -- complications
- Nervous System Diseases -- complications
- Renal Tubular Transport, Inborn Errors -- complications
- Sodium Potassium Chloride Symporter Inhibitors -- administration & dosage
- Solute Carrier Family 12, Member 3 -- genetics
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Publication Type: Case Reports; Journal Article
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