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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Detalles Bibliográficos
Autores principales: Rego, Teresa, Fonseca, Fernando, Cerqueira, Rita, Agapito, Ana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2018
Materias:
Unusual Association of Diseases/Symptoms
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5990061/
https://www.ncbi.nlm.nih.gov/pubmed/29871958
http://dx.doi.org/10.1136/bcr-2017-223663

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5990061/
https://www.ncbi.nlm.nih.gov/pubmed/29871958
http://dx.doi.org/10.1136/bcr-2017-223663

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