Concurrent Gitelman Syndrome-like Tubulopathy and Grave’s Disease

Gitelman syndrome (GS) is a rare autosomal recessive disorder characterized by the loss of function mutation of the solute carrier family-12 member-3 (SLC12A3) gene, encoding for sodium-chloride cotransporter of the distal convolute tubule. GS is characterized by hypokalemia, hypomagnesemia, metabol...

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Detalles Bibliográficos
Autores principales: Kumar, Rajasekaran Kishore, Srimathy, Venkatesh, Annigeri, Rajeev A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9267079/
https://www.ncbi.nlm.nih.gov/pubmed/35814325
http://dx.doi.org/10.4103/ijn.IJN_532_20

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9267079/
https://www.ncbi.nlm.nih.gov/pubmed/35814325
http://dx.doi.org/10.4103/ijn.IJN_532_20

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