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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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Bibliografski detalji
Glavni autori: Wojciech Wolyniec, Sonia Kaniuka- Jakubowska, Mato Nagel, Zuzanna Wolyniec, Lukasz Obolonczyk, Renata Swiatkowska-Stodulska, Krzysztof Sworczak, Marcin Renke
Format: Artigo
Jezik:Espanhol
Izdano: Elsevier 2016-05-01
Serija:Nefrología
Teme:
Online pristup:http://www.sciencedirect.com/science/article/pii/S0211699515000648
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