Periodontal manifestations of patients with Turner's syndrome: Report of 3 cases
Complete or partial absence of the second sex chromosome, with or without a mosaic karyotype, is detected in approximately 1 per 2,500 live-born females. Such a cytogenetic finding coupled with clinical features, such as short stature and ovarian failure, supports the diagnosis of Turner's synd...
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Veröffentlicht in: | Journal of Indian Society of Periodontology 2012-07, Vol.16 (3), p.451-455 |
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creator | Kasagani, Suresh Kumar Jampani, Narendra Dev Nutalapati, Rajasekhar Mutthineni, Ramesh Babu Ramisetti, Arpita |
description | Complete or partial absence of the second sex chromosome, with or without a mosaic karyotype, is detected in approximately 1 per 2,500 live-born females. Such a cytogenetic finding coupled with clinical features, such as short stature and ovarian failure, supports the diagnosis of Turner's syndrome (TS). It is typically characterized by the combination of physical features and cytogenetics in females. The presenting clinical features can vary widely among affected individuals. Consequently, whereas short stature and gonadal dysgenesis are almost universal in TS, many other organ systems are affected to varying degrees and at different stages of life. The periodontal status of three females diagnosed with TS has been reported here. |
doi_str_mv | 10.4103/0972-124X.100929 |
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Such a cytogenetic finding coupled with clinical features, such as short stature and ovarian failure, supports the diagnosis of Turner's syndrome (TS). It is typically characterized by the combination of physical features and cytogenetics in females. The presenting clinical features can vary widely among affected individuals. Consequently, whereas short stature and gonadal dysgenesis are almost universal in TS, many other organ systems are affected to varying degrees and at different stages of life. The periodontal status of three females diagnosed with TS has been reported here.</description><identifier>ISSN: 0972-124X</identifier><identifier>EISSN: 0975-1580</identifier><identifier>DOI: 10.4103/0972-124X.100929</identifier><identifier>PMID: 23162346</identifier><language>eng</language><publisher>India: Medknow Publications and Media Pvt. 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Such a cytogenetic finding coupled with clinical features, such as short stature and ovarian failure, supports the diagnosis of Turner's syndrome (TS). It is typically characterized by the combination of physical features and cytogenetics in females. The presenting clinical features can vary widely among affected individuals. Consequently, whereas short stature and gonadal dysgenesis are almost universal in TS, many other organ systems are affected to varying degrees and at different stages of life. The periodontal status of three females diagnosed with TS has been reported here.</description><subject>Abdomen</subject><subject>Care and treatment</subject><subject>Case Report</subject><subject>Case studies</subject><subject>Chromosomes</subject><subject>Dental care</subject><subject>Diagnosis</subject><subject>Enamel</subject><subject>Family medical history</subject><subject>Females</subject><subject>Fetuses</subject><subject>Growth hormones</subject><subject>Oral hygiene</subject><subject>Orthodontics</subject><subject>Periodontal disease</subject><subject>Teeth</subject><subject>Turner syndrome</subject><issn>0972-124X</issn><issn>0975-1580</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</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>eNptkctLAzEQxoMoVqt3T7Ig6GlrXs0mHgQRX1BQpIK3kGaTNrKb1GSr-N8b67Mgc8gw85uP-TIA7CE4oAiSYygqXCJMHwcIQoHFGtjKpWGJhhyuL_PPdg9sp_QEIaOcsE3QwwQxTCjbAnd3JrpQB9-ppmiVd9akTnUu-FQEW8xzanyXilfXzYrxInoTj1KR3nwdQ2tOinszD7H7QEmhVTJpB2xY1SSz-_X2wcPlxfj8uhzdXt2cn43KKa5oV2IuoNKIKjs0VGuOKsYZnVQaE87YkDBtoNXCqqrGVjOkkbIVU5QLJpCoLOmD00_d-WLSmlrnLaNq5Dy6VsU3GZSTqx3vZnIaXiShglcYZYGDL4EYnhfZtXwK2V_eWSLIBMZQQPxLTVVjpPM2ZDHduqTlGYEEcYoZydTgHypHbVqngzfW5frKwOGfgZlRTTdLoVksP34V3P9r88ff9wXJOwfwm-Y</recordid><startdate>201207</startdate><enddate>201207</enddate><creator>Kasagani, Suresh Kumar</creator><creator>Jampani, Narendra Dev</creator><creator>Nutalapati, Rajasekhar</creator><creator>Mutthineni, Ramesh Babu</creator><creator>Ramisetti, Arpita</creator><general>Medknow Publications and Media Pvt. 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Such a cytogenetic finding coupled with clinical features, such as short stature and ovarian failure, supports the diagnosis of Turner's syndrome (TS). It is typically characterized by the combination of physical features and cytogenetics in females. The presenting clinical features can vary widely among affected individuals. Consequently, whereas short stature and gonadal dysgenesis are almost universal in TS, many other organ systems are affected to varying degrees and at different stages of life. The periodontal status of three females diagnosed with TS has been reported here.</abstract><cop>India</cop><pub>Medknow Publications and Media Pvt. Ltd</pub><pmid>23162346</pmid><doi>10.4103/0972-124X.100929</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Abdomen Care and treatment Case Report Case studies Chromosomes Dental care Diagnosis Enamel Family medical history Females Fetuses Growth hormones Oral hygiene Orthodontics Periodontal disease Teeth Turner syndrome |
title | Periodontal manifestations of patients with Turner's syndrome: Report of 3 cases |
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