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Gitelman syndrome and primary hyperparathyroidism: a rare association
Gitelman syndrome(GS) is a rare autosomal recessive salt-losing tubulopathy of young adults, characterised by hypokalaemia, hypomagnesaemia, hypocalciuria and secondary hyperaldosteronism. Hypercalcaemia due to hypocalciuria in these patients is extremely rare. A 25-year-old healthy woman was referr...
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| Gepubliceerd in: | BMJ Case Rep |
|---|---|
| Hoofdauteurs: | , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
BMJ Publishing Group
2018
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5990061/ https://ncbi.nlm.nih.gov/pubmed/29871958 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2017-223663 |
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