Full Text
Full Text PDF
Abstract
The filtered load of water, electrolytes and toxic substances of human kidney is huge. The largest part of this filtered load must be absorbed by renal tubules. Our understanding of the transport mechanisms, their regulations and mechanism of action of diuretics has been increasing during the last decade. Recently, the genes of Bartter syndrome and Gitelman Syndrome were identified and mutations have been found which lead to these syndromes. These important findings makes the diagnosis of the two recessive syndromes easy.
Similar Articles
Article Info
Published In
Journal
Turkish Journal of Nephrology
Volume / Issue
Volume 7 · Issue 4
Pages
173-178
History
Published Online
March 20, 2019
Copyright
Copyright (c) 1998 Turkish Journal of Nephrology
Affiliations
Tayfun UÇAR
Ankara Üniversitesi Tıp Fakültesi Çocuk Sağlığı ve Hastalıkları ABD, Nefroloji Bilim Dalı, ANKARA
Fatoş YALÇINKAYA
Ankara Üniversitesi Tıp Fakültesi Çocuk Sağlığı ve Hastalıkları ABD, Nefroloji Bilim Dalı, ANKARA
Necmiye TURNER
Ankara Üniversitesi Tıp Fakültesi Çocuk Sağlığı ve Hastalıkları ABD, Nefroloji Bilim Dalı, ANKARA
Cite this Article
UÇAR, T., YALÇINKAYA, F., & TURNER, N. (2019). RENAL TUBULER TRANSPORT, DIURETICS AND GENETIC DEFECTS IN BARTTER AND GITELMAN SYNDROMES. Turkish Journal of Nephrology, 7(4), 173–178. Retrieved from https://www.turkjnephrol.org/index.php/pub/article/view/143
Outlines