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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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Détails bibliographiques
Publié dans:F1000Res
Auteurs principaux: Iqbal, Zahra, Mead, Paul, Sayer, John A.
Format: Artigo
Langue:Inglês
Publié: F1000Research 2016
Sujets:
Accès en ligne: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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