LEADER 03928nam 22007215 450 001 9910300235603321 005 20230328161011.0 010 $a3-319-13057-9 024 7 $a10.1007/978-3-319-13057-6 035 $a(CKB)3710000000356751 035 $a(EBL)1969312 035 $a(SSID)ssj0001452161 035 $a(PQKBManifestationID)11952149 035 $a(PQKBTitleCode)TC0001452161 035 $a(PQKBWorkID)11479941 035 $a(PQKB)11395593 035 $a(DE-He213)978-3-319-13057-6 035 $a(MiAaPQ)EBC1969312 035 $a(PPN)184494079 035 $a(EXLCZ)993710000000356751 100 $a20150209d2015 u| 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aCraniofacial and Dental Developmental Defects $eDiagnosis and Management /$fedited by J Timothy Wright 205 $a1st ed. 2015. 210 1$aCham :$cSpringer International Publishing :$cImprint: Springer,$d2015. 215 $a1 online resource (131 p.) 300 $aDescription based upon print version of record. 311 $a3-319-13056-0 320 $aIncludes bibliographical references at the end of each chapters and index. 327 $aIntroduction -- Failure of Tooth Eruption -- Non-Syndromic Hypodontia: Diagnosis and Treatment -- Syndromic Hypodontia ? Ectodermal Dysplasias -- Conditions Associated with Premature Tooth Exfoliation -- Defects of Enamel Development -- Defects of Dentin Development -- Managing the Cleft Patient -- Future Directions in Diagnosis and Treatment. 330 $aThis book is intended as a reference that will provide the practitioner with a framework for establishing a diagnosis and developing a suitable treatment plan in patients presenting with a range of developmental defects of the teeth. The conditions covered include failure of tooth eruption, hypodontia, premature tooth exfoliation, defects of enamel development, and defects of dentin development, with full consideration of both syndromic and non-syndromic defects. In each case the phenotype and genotype are first described, followed by diagnostic information, including the availability of genetic testing, and treatment options. Summarizing tables are used to highlight the key diagnostic features, and helpful illustrated case presentations are included. Cleft palate is also addressed, with details on etiology, phenotypes, treatment timing and approaches, and dental management. The closing chapter provides stimulating reflections on potential future directions in the diagnosis and treatment of these disorders, encompassing changes in management related to environmental?genetic interactions, tissue engineering, and materials. 606 $aDentistry 606 $aOral surgery 606 $aMaxilla$xSurgery 606 $aPediatrics 606 $aHuman genetics 606 $aDentistry$3https://scigraph.springernature.com/ontologies/product-market-codes/D00009 606 $aOral and Maxillofacial Surgery$3https://scigraph.springernature.com/ontologies/product-market-codes/H59060 606 $aPediatrics$3https://scigraph.springernature.com/ontologies/product-market-codes/H49006 606 $aHuman Genetics$3https://scigraph.springernature.com/ontologies/product-market-codes/B12008 615 0$aDentistry. 615 0$aOral surgery. 615 0$aMaxilla$xSurgery 615 0$aPediatrics. 615 0$aHuman genetics. 615 14$aDentistry. 615 24$aOral and Maxillofacial Surgery. 615 24$aPediatrics. 615 24$aHuman Genetics. 676 $a599935 676 $a611.01816 676 $a617.522059 676 $a617.6 676 $a618.92 702 $aWright$b J Timothy$4edt$4http://id.loc.gov/vocabulary/relators/edt 906 $aBOOK 912 $a9910300235603321 996 $aCraniofacial and Dental Developmental Defects$91760753 997 $aUNINA