Cargando…
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...
| Autores principales: | , , , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2012
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3470992/ https://www.ncbi.nlm.nih.gov/pubmed/23031616 http://dx.doi.org/10.1186/1752-1947-6-331 |