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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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| Publicat a: | F1000Res |
|---|---|
| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
F1000Research
2016
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| Matèries: | |
| Accés en línia: | 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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