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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...
Autores principales: | Rocha, João, Pacheco, Mariana, Matos, Mariana, Ferreira, Susana, Almeida, Jorge S |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2023
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Materias: | |
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 |
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