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...

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Detalles Bibliográficos
Autores principales: ALSaleh, Nourah, ALJurushi, Raghad, Alotaibi, Rakan, Alzahrani, Mohammed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Case Report
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

Internet

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

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