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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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| Publicado no: | J Nephropathol |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Society of Diabetic Nephropathy Prevention
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4417668/ https://ncbi.nlm.nih.gov/pubmed/25964887 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12860/jnp.2015.08 |
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