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Gitelman syndrome: A first published clinical association with chronic pancreatitis, a case report and review of literature
INTRODUCTION AND IMPORTANCE: Gitelman syndrome (GS) is an autosomal recessive, salt-losing tubulopathy, also referred to as familial hypokalemia-hypomagnesemia, caused by mutation of genes encoding the sodium chloride cotransporter (NCCT) and magnesium transporters in the thiazide sensitive segments...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Elsevier
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8801992/ https://www.ncbi.nlm.nih.gov/pubmed/35091353 http://dx.doi.org/10.1016/j.ijscr.2022.106779 |