Gitelman Syndrome: A Case Report

Gitelman syndrome is a rare hereditary tubulopathy characterized by hypokalemic metabolic alkalosis, hypomagnesemia, and hypocalciuria. In this case report, we describe a 21-year-old male who presented with myalgias, asthenia, general muscle weakness, and hypokalemia after receiving oral potassium s...

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Detalles Bibliográficos
Autores principales: Rocha, João, Pacheco, Mariana, Matos, Mariana, Ferreira, Susana, Almeida, Jorge S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10234615/
https://www.ncbi.nlm.nih.gov/pubmed/37273382
http://dx.doi.org/10.7759/cureus.38418

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10234615/
https://www.ncbi.nlm.nih.gov/pubmed/37273382
http://dx.doi.org/10.7759/cureus.38418

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