Gitelman Syndrome Provisionally Diagnosed During the First Presentation of Diabetic Ketoacidosis

Gitelman syndrome (GS) is an autosomal recessive disease characterized by hypokalemia, hypomagnesemia, metabolic alkalosis, and hypocalciuria. It is caused by mutations in gene SLC12A3 (located in chromosome 16q) encoding NaCl cotransporter. GS is usually asymptomatic for several years and is diagno...

Popoln opis

Shranjeno v:
Bibliografske podrobnosti
izdano v:Cureus
Main Authors: Jalalzadeh, Mojgan, Garcia Goncalves de Brito, David, Chaudhari, Shobhana, Poor, Armeen D, Baumstein, Donald
Format: Artigo
Jezik:Inglês
Izdano: Cureus 2021
Teme:
Endocrinology/Diabetes/Metabolism
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC8088595/
https://ncbi.nlm.nih.gov/pubmed/33954067
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7759/cureus.14253
Oznake: Označite
Brez oznak, prvi označite!

Podobne knjige/članki