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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| Veröffentlicht in: | Indian journal of nephrology 2017-09, Vol.27 (5), p.399-401 |
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| container_title | Indian journal of nephrology |
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| creator | 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 |
| 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. |
| doi_str_mv | 10.4103/ijn.IJN_203_16 |
| format | Article |
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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.</description><identifier>ISSN: 0971-4065</identifier><identifier>EISSN: 1998-3662</identifier><identifier>DOI: 10.4103/ijn.IJN_203_16</identifier><identifier>PMID: 28904439</identifier><language>eng</language><publisher>India: Medknow Publications and Media Pvt. Ltd</publisher><subject>Amelogenesis imperfecta ; Blood pressure ; Case Report ; Constipation ; Defects ; Dental enamel ; Enamel ; Genetic aspects ; Hyperaldosteronism ; Kidney diseases ; Medicine ; Nephrology ; Patients ; Potassium ; Proteins ; Teeth</subject><ispartof>Indian journal of nephrology, 2017-09, Vol.27 (5), p.399-401</ispartof><rights>COPYRIGHT 2017 Medknow Publications and Media Pvt. Ltd.</rights><rights>Copyright Medknow Publications & Media Pvt. Ltd. Sep/Oct 2017</rights><rights>Copyright: © 2017 Indian Journal of Nephrology 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3986-8e8a1988d5966640dceb4ebf661db132338e2f02ee27704f04df160cc40b2b8d3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5590420/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5590420/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28904439$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kumar, A C V</creatorcontrib><creatorcontrib>Alekya, V</creatorcontrib><creatorcontrib>Krishna, M S V V</creatorcontrib><creatorcontrib>Alekya, K</creatorcontrib><creatorcontrib>Aruna, M</creatorcontrib><creatorcontrib>Reddy, M H K</creatorcontrib><creatorcontrib>Sangeetha, B</creatorcontrib><creatorcontrib>Ram, R</creatorcontrib><creatorcontrib>Kumar, V S</creatorcontrib><title>Association of Amelogenesis Imperfecta and Bartter's Syndrome</title><title>Indian journal of nephrology</title><addtitle>Indian J Nephrol</addtitle><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.</description><subject>Amelogenesis imperfecta</subject><subject>Blood pressure</subject><subject>Case Report</subject><subject>Constipation</subject><subject>Defects</subject><subject>Dental enamel</subject><subject>Enamel</subject><subject>Genetic aspects</subject><subject>Hyperaldosteronism</subject><subject>Kidney diseases</subject><subject>Medicine</subject><subject>Nephrology</subject><subject>Patients</subject><subject>Potassium</subject><subject>Proteins</subject><subject>Teeth</subject><issn>0971-4065</issn><issn>1998-3662</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNptUU1rGzEQFaGhcZxecywLhfa0jr5Wlg4tOCFtHEJ6aHsWWu3IltmVHGkdyL-vTNN8QJjDwMx7j5n3EDoleMYJZmd-E2bL61tNMdNEHKAJUUrWTAj6Dk2wmpOaY9EcoeOcNxjThqvmPTqiUmHOmZqgr4uco_Vm9DFU0VWLAfq4ggDZ52o5bCE5sKOpTOiqc5PGEdKXXP16CF2KA5ygQ2f6DB8e-xT9-X75--Kqvvn5Y3mxuKktU1LUEqQhSsquUUIIjjsLLYfWCUG6ljDKmATqMAWg8znmDvPOEYGt5bilrezYFH37p7vdtQMUehiT6fU2-cGkBx2N1683wa_1Kt7rpimPFm-m6NOjQIp3O8ij3sRdCuVmTZRgxQzBm2fUyvSgfXCxiNnBZ6sXDeF0Lonco2ZvoEp1MHgbAzhf5q8In18Q1mD6cZ1jv9t7nt9UtinmnMA9fUiw3setS9z6Oe5C-PjSlyf4_3zZX9sTpLU</recordid><startdate>20170901</startdate><enddate>20170901</enddate><creator>Kumar, A C V</creator><creator>Alekya, V</creator><creator>Krishna, M S V V</creator><creator>Alekya, K</creator><creator>Aruna, M</creator><creator>Reddy, M H K</creator><creator>Sangeetha, B</creator><creator>Ram, R</creator><creator>Kumar, V S</creator><general>Medknow Publications and Media Pvt. 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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.</abstract><cop>India</cop><pub>Medknow Publications and Media Pvt. Ltd</pub><pmid>28904439</pmid><doi>10.4103/ijn.IJN_203_16</doi><tpages>3</tpages><oa>free_for_read</oa></addata></record> |
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| source | Medknow Open Access Journals; EZB-FREE-00999 freely available EZB journals; PubMed Central |
| subjects | Amelogenesis imperfecta Blood pressure Case Report Constipation Defects Dental enamel Enamel Genetic aspects Hyperaldosteronism Kidney diseases Medicine Nephrology Patients Potassium Proteins Teeth |
| title | Association of Amelogenesis Imperfecta and Bartter's Syndrome |
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