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Heart’s Dangerous Symphony: Torsade De Pointes Unleashed by Gitelman Syndrome-Induced Hypomagnesemia

Gitelman syndrome (GS) is a rare autosomal recessive salt-losing renal tubular disorder associated with a mutation of SLC12A3 or CLCNKB genes which encodes the thiazide-sensitive sodium-chloride co-transporter (NCCT) in the distal renal tubule. It is inherited as an autosomal recessive disorder. Hyp...

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Detalles Bibliográficos
Autores principales: Idries, Iyad Y, Azhar, Muhammad, Yadav, Ruchi, Nevolina, Anna, Ullah, Abid, Sur, Avtar, Zadoretska, Iryna, Gunsburg, Moshe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10544222/
https://www.ncbi.nlm.nih.gov/pubmed/37791211
http://dx.doi.org/10.7759/cureus.44464