RF30 | PSAT136 Gitelman Syndrome and Primary Hyperparathyroidism, a Case Report

INTRODUCTION: Gitelman syndrome, also known as familial hypokalemia-hypomagnesemia, is a rare autosomal recessive disorder that impairs the sodium chloride cotransporter (NCC) and magnesium channels in the renal distal convoluted tubule, causing salt-losing tubulopathy. It is characterized by hypoka...

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Detalles Bibliográficos
Autores principales: Alnahas, Zeinab, Markov, Marko, Horani, Mohamad H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Genetics & Development
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9625697/
http://dx.doi.org/10.1210/jendso/bvac150.968

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9625697/
http://dx.doi.org/10.1210/jendso/bvac150.968

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