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Gitelman syndrome manifesting in early childhood and leading to delayed puberty: a case report
INTRODUCTION: Gitelman syndrome is an inherited autosomal recessive renal salt-wasting disorder. It presents with variable clinical symptoms including muscle weakness and fatigue, and the diagnosis is based on metabolic alkalosis, hypokalemia, hypomagnesemia and hypocalciuria. It is usually diagnose...
Gorde:
| Egile Nagusiak: | , , , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
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BioMed Central
2012
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3470992/ https://ncbi.nlm.nih.gov/pubmed/23031616 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1752-1947-6-331 |
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