Acquired Gitelman Syndrome Associated with Systemic Sclerosis

Gitelman syndrome is an inherited renal disorder characterized by hypomagnesemia, hypokalemia, hypocalciuria and metabolic alkalosis linked to the genes encoding the thiazide sensitive NaCl cotransporter (NCCT) located on the distal convoluted tubule of the kidney. It usually presents in late childh...

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Detalles Bibliográficos
Autores principales: Masab, Muhammad, Goyal, Abhinav, Abrol, Surbhi, Rangaswami, Janani
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2019
Materias:
Internal Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6430306/
https://www.ncbi.nlm.nih.gov/pubmed/30931194
http://dx.doi.org/10.7759/cureus.3923

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6430306/
https://www.ncbi.nlm.nih.gov/pubmed/30931194
http://dx.doi.org/10.7759/cureus.3923

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