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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...
Autores principales: | Rego, Teresa, Fonseca, Fernando, Cerqueira, Rita, Agapito, Ana |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2018
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Materias: | |
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 |
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