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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Detalles Bibliográficos
Autores principales: Iqbal, Zahra, Mead, Paul, Sayer, John A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000Research 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4897758/
https://www.ncbi.nlm.nih.gov/pubmed/27303630
http://dx.doi.org/10.12688/f1000research.8732.1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4897758/
https://www.ncbi.nlm.nih.gov/pubmed/27303630
http://dx.doi.org/10.12688/f1000research.8732.1

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