A case report of Gitelman syndrome resulting from two novel mutations in SLC12A3 gene

A case report of Gitelman syndrome resulting from two novel mutations in SLC12A3 gene

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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 histor...

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Bibliographic Details
Main Authors: Wojciech Wolyniec, Sonia Kaniuka- Jakubowska, Mato Nagel, Zuzanna Wolyniec, Lukasz Obolonczyk, Renata Swiatkowska-Stodulska, Krzysztof Sworczak, Marcin Renke
Format: Article
Language:English
Published: Elsevier 2016-05-01
Series:Nefrología (English Edition)
Subjects:
Hypokalaemia
Hypomagnesaemia
Diuretics
Online Access:http://www.sciencedirect.com/science/article/pii/S2013251415000656

Internet

http://www.sciencedirect.com/science/article/pii/S2013251415000656

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