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Attenuated renal excretion in response to thiazide diuretics in Gitelman's syndrome: a case report.

Gitelman's syndrome is a variant of Bartter's syndrome characterized by hypocalciuria and hypomagnesemia. The administration of thiazide diuretics may induce a subnormal increase of urinary Na+ and Cl- excretion in patients with Gitelman's syndrome, consistent with the hypothesis that...

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Autores principales: Yeum, Chung-Ho, Kim, Soo-Wan, Ma, Seong-Kwon, Ko, Jung-Hee, Nah, Myong-Yun, Kim, Nam-Ho, Choi, Ki-Chul
Formato: Texto
Lenguaje:English
Publicado: Korean Academy of Medical Sciences 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054904/
https://www.ncbi.nlm.nih.gov/pubmed/12172059
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author Yeum, Chung-Ho
Kim, Soo-Wan
Ma, Seong-Kwon
Ko, Jung-Hee
Nah, Myong-Yun
Kim, Nam-Ho
Choi, Ki-Chul
author_facet Yeum, Chung-Ho
Kim, Soo-Wan
Ma, Seong-Kwon
Ko, Jung-Hee
Nah, Myong-Yun
Kim, Nam-Ho
Choi, Ki-Chul
author_sort Yeum, Chung-Ho
collection PubMed
description Gitelman's syndrome is a variant of Bartter's syndrome characterized by hypocalciuria and hypomagnesemia. The administration of thiazide diuretics may induce a subnormal increase of urinary Na+ and Cl- excretion in patients with Gitelman's syndrome, consistent with the hypothesis that less Na+ and Cl- than normal is reabsorbed by the thiazide-inhibitable transporter in Gitelman's syndrome. Specific mutations of NaCl cotransporter, coupled with mutant NaCl cotransporter expression studies clearly demonstrated that many of the characteristics of individuals with Gitelman's syndrome are explained by lack of function of NaCl cotransporter. We recently diagnosed a patient with Gitelman's syndrome by performing the thiazide and furosemide tests, and it is suggested that the clearance studies by diuretic administration may be of diagnostic help in Gitelman's syndrome.
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spelling pubmed-30549042011-03-15 Attenuated renal excretion in response to thiazide diuretics in Gitelman's syndrome: a case report. Yeum, Chung-Ho Kim, Soo-Wan Ma, Seong-Kwon Ko, Jung-Hee Nah, Myong-Yun Kim, Nam-Ho Choi, Ki-Chul J Korean Med Sci Research Article Gitelman's syndrome is a variant of Bartter's syndrome characterized by hypocalciuria and hypomagnesemia. The administration of thiazide diuretics may induce a subnormal increase of urinary Na+ and Cl- excretion in patients with Gitelman's syndrome, consistent with the hypothesis that less Na+ and Cl- than normal is reabsorbed by the thiazide-inhibitable transporter in Gitelman's syndrome. Specific mutations of NaCl cotransporter, coupled with mutant NaCl cotransporter expression studies clearly demonstrated that many of the characteristics of individuals with Gitelman's syndrome are explained by lack of function of NaCl cotransporter. We recently diagnosed a patient with Gitelman's syndrome by performing the thiazide and furosemide tests, and it is suggested that the clearance studies by diuretic administration may be of diagnostic help in Gitelman's syndrome. Korean Academy of Medical Sciences 2002-08 /pmc/articles/PMC3054904/ /pubmed/12172059 Text en
spellingShingle Research Article
Yeum, Chung-Ho
Kim, Soo-Wan
Ma, Seong-Kwon
Ko, Jung-Hee
Nah, Myong-Yun
Kim, Nam-Ho
Choi, Ki-Chul
Attenuated renal excretion in response to thiazide diuretics in Gitelman's syndrome: a case report.
title Attenuated renal excretion in response to thiazide diuretics in Gitelman's syndrome: a case report.
title_full Attenuated renal excretion in response to thiazide diuretics in Gitelman's syndrome: a case report.
title_fullStr Attenuated renal excretion in response to thiazide diuretics in Gitelman's syndrome: a case report.
title_full_unstemmed Attenuated renal excretion in response to thiazide diuretics in Gitelman's syndrome: a case report.
title_short Attenuated renal excretion in response to thiazide diuretics in Gitelman's syndrome: a case report.
title_sort attenuated renal excretion in response to thiazide diuretics in gitelman's syndrome: a case report.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054904/
https://www.ncbi.nlm.nih.gov/pubmed/12172059
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