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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

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