A case report of Gitelman syndrome resulting from two novel mutations in SLC12A3 gene
Introduction: Hypokalaemia is a common clinical problem. A potential but commonly overlooked cause of hypokalaemia is Gitelman syndrome. Material and methods: A 26-year-old man was admitted to the hospital due to syncope with general and muscular weakness and muscle cramps. The patient's history rev...
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| Autors principals: | , , , , , , , |
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| Format: | Artigo |
| Idioma: | Espanhol |
| Publicat: |
Elsevier
2016-05-01
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| Col·lecció: | Nefrología |
| Matèries: | |
| Accés en línia: | http://www.sciencedirect.com/science/article/pii/S0211699515000648 |
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