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Dental anomalies in Richieri-Costa-Pereira syndrome
Objective The objective of this study was to investigate the prevalence of dental anomalies in individuals with Richieri-Costa-Pereira syndrome. Study Design A total of 13 individuals with Richieri-Costa-Pereira syndrome who were older than 8 years with at least 1 available panoramic radiograph were...
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Published in: | Oral surgery, oral medicine, oral pathology and oral radiology oral medicine, oral pathology and oral radiology, 2012-07, Vol.114 (1), p.99-106 |
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creator | Severini, Janete Mary Baaclini Galante, DDS, MSc, PhD da Silva Dalben, Gisele, DDS, MSc, PhD Richieri-Costa, Antonio, MD, MSc, PhD Ozawa, Terumi Okada, DDS, MSc, PhD |
description | Objective The objective of this study was to investigate the prevalence of dental anomalies in individuals with Richieri-Costa-Pereira syndrome. Study Design A total of 13 individuals with Richieri-Costa-Pereira syndrome who were older than 8 years with at least 1 available panoramic radiograph were assessed. Dental anomalies were evaluated clinically and radiographically and classified as hyperplastic, hypoplastic, or heterotopic and as alterations of shape, number, position, and structure. Enamel alterations were classified by the DDE index. Results All individuals exhibited anomalies, with predominance of hypoplastic disorders, mainly agenesis of mandibular incisors and second premolars and demarcated creamy-white enamel opacities primarily affecting the maxillary premolars. Conclusions Individuals with Richieri-Costa Pereira syndrome exhibit high prevalence of tooth agenesis, especially mandibular incisors and premolars, as well as high frequency of enamel opacities. These findings are compatible with the mandibular cleft observed in all individuals and also reflect the hypoplastic characteristic of the syndrome. |
doi_str_mv | 10.1016/j.oooo.2012.03.009 |
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Study Design A total of 13 individuals with Richieri-Costa-Pereira syndrome who were older than 8 years with at least 1 available panoramic radiograph were assessed. Dental anomalies were evaluated clinically and radiographically and classified as hyperplastic, hypoplastic, or heterotopic and as alterations of shape, number, position, and structure. Enamel alterations were classified by the DDE index. Results All individuals exhibited anomalies, with predominance of hypoplastic disorders, mainly agenesis of mandibular incisors and second premolars and demarcated creamy-white enamel opacities primarily affecting the maxillary premolars. Conclusions Individuals with Richieri-Costa Pereira syndrome exhibit high prevalence of tooth agenesis, especially mandibular incisors and premolars, as well as high frequency of enamel opacities. These findings are compatible with the mandibular cleft observed in all individuals and also reflect the hypoplastic characteristic of the syndrome.</description><identifier>ISSN: 2212-4403</identifier><identifier>EISSN: 2212-4411</identifier><identifier>DOI: 10.1016/j.oooo.2012.03.009</identifier><identifier>PMID: 22727098</identifier><language>eng</language><publisher>New York, NY: Mosby, Inc</publisher><subject>Adolescent ; Adult ; Biological and medical sciences ; Child ; Clubfoot - complications ; Dentistry ; Female ; Hand Deformities, Congenital - complications ; Humans ; Male ; Medical sciences ; Otorhinolaryngology. Stomatology ; Pierre Robin Syndrome - complications ; Radiography, Panoramic ; Surgery ; Tooth Abnormalities - diagnosis</subject><ispartof>Oral surgery, oral medicine, oral pathology and oral radiology, 2012-07, Vol.114 (1), p.99-106</ispartof><rights>Mosby, Inc.</rights><rights>2012 Mosby, Inc.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2012 Mosby, Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c441t-e65342a7f5587b2ac35d9babc6ffd75b966f6f9b4e6bc09763c352225e9742d53</citedby><cites>FETCH-LOGICAL-c441t-e65342a7f5587b2ac35d9babc6ffd75b966f6f9b4e6bc09763c352225e9742d53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26099369$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22727098$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Severini, Janete Mary Baaclini Galante, DDS, MSc, PhD</creatorcontrib><creatorcontrib>da Silva Dalben, Gisele, DDS, MSc, PhD</creatorcontrib><creatorcontrib>Richieri-Costa, Antonio, MD, MSc, PhD</creatorcontrib><creatorcontrib>Ozawa, Terumi Okada, DDS, MSc, PhD</creatorcontrib><title>Dental anomalies in Richieri-Costa-Pereira syndrome</title><title>Oral surgery, oral medicine, oral pathology and oral radiology</title><addtitle>Oral Surg Oral Med Oral Pathol Oral Radiol</addtitle><description>Objective The objective of this study was to investigate the prevalence of dental anomalies in individuals with Richieri-Costa-Pereira syndrome. Study Design A total of 13 individuals with Richieri-Costa-Pereira syndrome who were older than 8 years with at least 1 available panoramic radiograph were assessed. Dental anomalies were evaluated clinically and radiographically and classified as hyperplastic, hypoplastic, or heterotopic and as alterations of shape, number, position, and structure. Enamel alterations were classified by the DDE index. Results All individuals exhibited anomalies, with predominance of hypoplastic disorders, mainly agenesis of mandibular incisors and second premolars and demarcated creamy-white enamel opacities primarily affecting the maxillary premolars. Conclusions Individuals with Richieri-Costa Pereira syndrome exhibit high prevalence of tooth agenesis, especially mandibular incisors and premolars, as well as high frequency of enamel opacities. These findings are compatible with the mandibular cleft observed in all individuals and also reflect the hypoplastic characteristic of the syndrome.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Clubfoot - complications</subject><subject>Dentistry</subject><subject>Female</subject><subject>Hand Deformities, Congenital - complications</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Otorhinolaryngology. Stomatology</subject><subject>Pierre Robin Syndrome - complications</subject><subject>Radiography, Panoramic</subject><subject>Surgery</subject><subject>Tooth Abnormalities - diagnosis</subject><issn>2212-4403</issn><issn>2212-4411</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNp9kcFq3DAQhkVoaEKSF-gh-FLoxY40suUVhELZNkkhkJC0ZyHLI6qtLSWSXdi3r8xuEuihc5EO3z8zfEPIB0YrRpm42FQhVwWUQUV5Rak8IMcADMq6Zuzd65_yI3KW0obmEjlYw3tyBNBCS-XqmPCv6Cc9FNqHUQ8OU-F88eDML4fRleuQJl3eY0QXdZG2vo9hxFNyaPWQ8Gz_npCfV99-rG_K27vr7-svt6XJK0wliobXoFvbNKu2A21408tOd0ZY27dNJ4WwwsquRtEZKlvBMwEADcq2hr7hJ-TTru9TDM8zpkmNLhkcBu0xzEkxmmlBpaQZhR1qYkgpolVP0Y06bjOkFl9qoxZfavGlKFfZVw6d7_vP3Yj9a-TFTgY-7gGdjB5s1N649MYts7lYGl3uOMw2_mRzKhmH3mDvIppJ9cH9f4_P_8TN4LzLE3_jFtMmzNFnz4qplDPqcbnsclgGlMJKCP4XrWCb1g</recordid><startdate>20120701</startdate><enddate>20120701</enddate><creator>Severini, Janete Mary Baaclini Galante, DDS, MSc, PhD</creator><creator>da Silva Dalben, Gisele, DDS, MSc, PhD</creator><creator>Richieri-Costa, Antonio, MD, MSc, PhD</creator><creator>Ozawa, Terumi Okada, DDS, MSc, PhD</creator><general>Mosby, Inc</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20120701</creationdate><title>Dental anomalies in Richieri-Costa-Pereira syndrome</title><author>Severini, Janete Mary Baaclini Galante, DDS, MSc, PhD ; da Silva Dalben, Gisele, DDS, MSc, PhD ; Richieri-Costa, Antonio, MD, MSc, PhD ; Ozawa, Terumi Okada, DDS, MSc, PhD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c441t-e65342a7f5587b2ac35d9babc6ffd75b966f6f9b4e6bc09763c352225e9742d53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Clubfoot - complications</topic><topic>Dentistry</topic><topic>Female</topic><topic>Hand Deformities, Congenital - complications</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Otorhinolaryngology. Stomatology</topic><topic>Pierre Robin Syndrome - complications</topic><topic>Radiography, Panoramic</topic><topic>Surgery</topic><topic>Tooth Abnormalities - diagnosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Severini, Janete Mary Baaclini Galante, DDS, MSc, PhD</creatorcontrib><creatorcontrib>da Silva Dalben, Gisele, DDS, MSc, PhD</creatorcontrib><creatorcontrib>Richieri-Costa, Antonio, MD, MSc, PhD</creatorcontrib><creatorcontrib>Ozawa, Terumi Okada, DDS, MSc, PhD</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Oral surgery, oral medicine, oral pathology and oral radiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Severini, Janete Mary Baaclini Galante, DDS, MSc, PhD</au><au>da Silva Dalben, Gisele, DDS, MSc, PhD</au><au>Richieri-Costa, Antonio, MD, MSc, PhD</au><au>Ozawa, Terumi Okada, DDS, MSc, PhD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dental anomalies in Richieri-Costa-Pereira syndrome</atitle><jtitle>Oral surgery, oral medicine, oral pathology and oral radiology</jtitle><addtitle>Oral Surg Oral Med Oral Pathol Oral Radiol</addtitle><date>2012-07-01</date><risdate>2012</risdate><volume>114</volume><issue>1</issue><spage>99</spage><epage>106</epage><pages>99-106</pages><issn>2212-4403</issn><eissn>2212-4411</eissn><abstract>Objective The objective of this study was to investigate the prevalence of dental anomalies in individuals with Richieri-Costa-Pereira syndrome. Study Design A total of 13 individuals with Richieri-Costa-Pereira syndrome who were older than 8 years with at least 1 available panoramic radiograph were assessed. Dental anomalies were evaluated clinically and radiographically and classified as hyperplastic, hypoplastic, or heterotopic and as alterations of shape, number, position, and structure. Enamel alterations were classified by the DDE index. Results All individuals exhibited anomalies, with predominance of hypoplastic disorders, mainly agenesis of mandibular incisors and second premolars and demarcated creamy-white enamel opacities primarily affecting the maxillary premolars. Conclusions Individuals with Richieri-Costa Pereira syndrome exhibit high prevalence of tooth agenesis, especially mandibular incisors and premolars, as well as high frequency of enamel opacities. These findings are compatible with the mandibular cleft observed in all individuals and also reflect the hypoplastic characteristic of the syndrome.</abstract><cop>New York, NY</cop><pub>Mosby, Inc</pub><pmid>22727098</pmid><doi>10.1016/j.oooo.2012.03.009</doi><tpages>8</tpages></addata></record> |
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subjects | Adolescent Adult Biological and medical sciences Child Clubfoot - complications Dentistry Female Hand Deformities, Congenital - complications Humans Male Medical sciences Otorhinolaryngology. Stomatology Pierre Robin Syndrome - complications Radiography, Panoramic Surgery Tooth Abnormalities - diagnosis |
title | Dental anomalies in Richieri-Costa-Pereira syndrome |
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