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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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Bibliografische gegevens
Gepubliceerd in:BMJ Case Rep
Hoofdauteurs: Rego, Teresa, Fonseca, Fernando, Cerqueira, Rita, Agapito, Ana
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: BMJ Publishing Group 2018
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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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