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Gitelman’s syndrome complicated by mild renal insufficiency and high anion gap acidosis; a rare presentation in a young female

Background: Gitelman’s syndrome (GS) is a rare autosomal recessive renal tubular disorder that is characterized by episodic clinical manifestations and persistent biochemical abnormalities. The disorder manifests in adolescent or adult age and is characterized by transient episodes of muscle weaknes...

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Detalles Bibliográficos
Autores principales: Hassan Jafry, Nazrul, Ahmed, Ejaz, Mubarak, Muhammed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society of Diabetic Nephropathy Prevention 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4417668/
https://www.ncbi.nlm.nih.gov/pubmed/25964887
http://dx.doi.org/10.12860/jnp.2015.08

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