Molecular Basis, Diagnostic Challenges and Therapeutic Approaches of Bartter and Gitelman Syndromes: A Primer for Clinicians

Gitelman and Bartter syndromes are rare inherited diseases that belong to the category of renal tubulopathies. The genes associated with these pathologies encode electrolyte transport proteins located in the nephron, particularly in the Distal Convoluted Tubule and Ascending Loop of Henle. Therefore...

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Detalles Bibliográficos
Autores principales: Nuñez-Gonzalez, Laura, Carrera, Noa, Garcia-Gonzalez, Miguel A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8584233/
https://www.ncbi.nlm.nih.gov/pubmed/34768847
http://dx.doi.org/10.3390/ijms222111414

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8584233/
https://www.ncbi.nlm.nih.gov/pubmed/34768847
http://dx.doi.org/10.3390/ijms222111414

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