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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...
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| Main Authors: | , , , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
BioMed Central
2012
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| Fag: | |
| Online adgang: | 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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