Association of Amelogenesis Imperfecta and Bartter's Syndrome

Bartter's syndrome is an autosomal recessive renal tubular disorder characterized by hypokalemia, hypochloremia, metabolic alkalosis, and hyperreninemia with normal blood pressure. Bartter's syndrome is associated with hypercalciuria and nephrocalcinosis. Amelogenesis imperfecta (AI) is a...

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Autores principales: Kumar, A. C. V., Alekya, V., Krishna, M. S. V. V., Alekya, K., Aruna, M., Reddy, M. H. K., Sangeetha, B., Ram, R., Kumar, V. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5590420/
https://www.ncbi.nlm.nih.gov/pubmed/28904439
http://dx.doi.org/10.4103/ijn.IJN_203_16
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author Kumar, A. C. V.
Alekya, V.
Krishna, M. S. V. V.
Alekya, K.
Aruna, M.
Reddy, M. H. K.
Sangeetha, B.
Ram, R.
Kumar, V. S.
author_facet Kumar, A. C. V.
Alekya, V.
Krishna, M. S. V. V.
Alekya, K.
Aruna, M.
Reddy, M. H. K.
Sangeetha, B.
Ram, R.
Kumar, V. S.
author_sort Kumar, A. C. V.
collection PubMed
description Bartter's syndrome is an autosomal recessive renal tubular disorder characterized by hypokalemia, hypochloremia, metabolic alkalosis, and hyperreninemia with normal blood pressure. Bartter's syndrome is associated with hypercalciuria and nephrocalcinosis. Amelogenesis imperfecta (AI) is a group of hereditary disorders that affect dental enamel. AI could be part of several syndromes. The enamel renal syndrome is the association of AI and nephrocalcinosis. We report two patients of AI with Bartter's syndrome.
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spelling pubmed-55904202017-09-13 Association of Amelogenesis Imperfecta and Bartter's Syndrome Kumar, A. C. V. Alekya, V. Krishna, M. S. V. V. Alekya, K. Aruna, M. Reddy, M. H. K. Sangeetha, B. Ram, R. Kumar, V. S. Indian J Nephrol Case Report Bartter's syndrome is an autosomal recessive renal tubular disorder characterized by hypokalemia, hypochloremia, metabolic alkalosis, and hyperreninemia with normal blood pressure. Bartter's syndrome is associated with hypercalciuria and nephrocalcinosis. Amelogenesis imperfecta (AI) is a group of hereditary disorders that affect dental enamel. AI could be part of several syndromes. The enamel renal syndrome is the association of AI and nephrocalcinosis. We report two patients of AI with Bartter's syndrome. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5590420/ /pubmed/28904439 http://dx.doi.org/10.4103/ijn.IJN_203_16 Text en Copyright: © 2017 Indian Journal of Nephrology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report
Kumar, A. C. V.
Alekya, V.
Krishna, M. S. V. V.
Alekya, K.
Aruna, M.
Reddy, M. H. K.
Sangeetha, B.
Ram, R.
Kumar, V. S.
Association of Amelogenesis Imperfecta and Bartter's Syndrome
title Association of Amelogenesis Imperfecta and Bartter's Syndrome
title_full Association of Amelogenesis Imperfecta and Bartter's Syndrome
title_fullStr Association of Amelogenesis Imperfecta and Bartter's Syndrome
title_full_unstemmed Association of Amelogenesis Imperfecta and Bartter's Syndrome
title_short Association of Amelogenesis Imperfecta and Bartter's Syndrome
title_sort association of amelogenesis imperfecta and bartter's syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5590420/
https://www.ncbi.nlm.nih.gov/pubmed/28904439
http://dx.doi.org/10.4103/ijn.IJN_203_16
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