A Case of Gitelman Syndrome with Hypercalcemia Secondary to Primary Hyperparathyroidism

Gitelman syndrome is a rare autosomal recessive salt-losing tubulopathy characterized by hypokalemia, hypomagnesemia, hypocalciuria, and secondary hyperaldosteronism. However, hypercalcemia secondary to hypocalciuria is extremely rare during the disease. A 36-year-old normotensive man who suffered a...

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Detalles Bibliográficos
Autores principales: Alnahas, Zeinab, Markov, Marko, Horani, Mohamad H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9252710/
https://www.ncbi.nlm.nih.gov/pubmed/35795477
http://dx.doi.org/10.1155/2022/1098222

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9252710/
https://www.ncbi.nlm.nih.gov/pubmed/35795477
http://dx.doi.org/10.1155/2022/1098222

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