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Acquired Gitelman Syndrome Associated with Systemic Sclerosis
Gitelman syndrome is an inherited renal disorder characterized by hypomagnesemia, hypokalemia, hypocalciuria and metabolic alkalosis linked to the genes encoding the thiazide sensitive NaCl cotransporter (NCCT) located on the distal convoluted tubule of the kidney. It usually presents in late childh...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6430306/ https://www.ncbi.nlm.nih.gov/pubmed/30931194 http://dx.doi.org/10.7759/cureus.3923 |
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author | Masab, Muhammad Goyal, Abhinav Abrol, Surbhi Rangaswami, Janani |
author_facet | Masab, Muhammad Goyal, Abhinav Abrol, Surbhi Rangaswami, Janani |
author_sort | Masab, Muhammad |
collection | PubMed |
description | Gitelman syndrome is an inherited renal disorder characterized by hypomagnesemia, hypokalemia, hypocalciuria and metabolic alkalosis linked to the genes encoding the thiazide sensitive NaCl cotransporter (NCCT) located on the distal convoluted tubule of the kidney. It usually presents in late childhood or early adulthood with electrolyte abnormalities resembling chronic thiazide diuretic use. Acquired Gitelman syndrome is a very rare disorder mostly associated with Sjogren’s syndrome. |
format | Online Article Text |
id | pubmed-6430306 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
spelling | pubmed-64303062019-03-29 Acquired Gitelman Syndrome Associated with Systemic Sclerosis Masab, Muhammad Goyal, Abhinav Abrol, Surbhi Rangaswami, Janani Cureus Internal Medicine Gitelman syndrome is an inherited renal disorder characterized by hypomagnesemia, hypokalemia, hypocalciuria and metabolic alkalosis linked to the genes encoding the thiazide sensitive NaCl cotransporter (NCCT) located on the distal convoluted tubule of the kidney. It usually presents in late childhood or early adulthood with electrolyte abnormalities resembling chronic thiazide diuretic use. Acquired Gitelman syndrome is a very rare disorder mostly associated with Sjogren’s syndrome. Cureus 2019-01-20 /pmc/articles/PMC6430306/ /pubmed/30931194 http://dx.doi.org/10.7759/cureus.3923 Text en Copyright © 2019, Masab et al. http://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Internal Medicine Masab, Muhammad Goyal, Abhinav Abrol, Surbhi Rangaswami, Janani Acquired Gitelman Syndrome Associated with Systemic Sclerosis |
title | Acquired Gitelman Syndrome Associated with Systemic Sclerosis |
title_full | Acquired Gitelman Syndrome Associated with Systemic Sclerosis |
title_fullStr | Acquired Gitelman Syndrome Associated with Systemic Sclerosis |
title_full_unstemmed | Acquired Gitelman Syndrome Associated with Systemic Sclerosis |
title_short | Acquired Gitelman Syndrome Associated with Systemic Sclerosis |
title_sort | acquired gitelman syndrome associated with systemic sclerosis |
topic | Internal Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6430306/ https://www.ncbi.nlm.nih.gov/pubmed/30931194 http://dx.doi.org/10.7759/cureus.3923 |
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