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Case Report: Cervical chondrocalcinosis as a complication of Gitelman syndrome
Gitelman syndrome is an inherited tubulopathy leading to a hypokalaemic metabolic alkalosis with hypomagnesaemia and hypocalciuria. Most cases are due to mutations in SLC12A3, encoding the apical thiazide sensitive co-transporter in the distal convoluted tubule. Musculoskeletal effects of Gitelman s...
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| Vydáno v: | F1000Res |
|---|---|
| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
F1000Research
2016
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4897758/ https://ncbi.nlm.nih.gov/pubmed/27303630 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12688/f1000research.8732.1 |
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