Gotowe bibliografie tematyczne / Tooth Anomalies

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Gotowa bibliografia na temat „Tooth Anomalies”

Autor: Grafiati

Data publikacji: 5 czerwca 2025

Data aktualizacji: 2 sierpnia 2025

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Artykuły w czasopismach na temat "Tooth Anomalies"

Kramerová, L., P. Krejčí, E. Kaplová, and K. Langová. "Tooth Agenesis and Associated Tooth Developmental Anomalies." Česká stomatologie/Praktické zubní lékařství 114, no. 1 (2014): 9–14. http://dx.doi.org/10.51479/cspzl.2014.026.

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Chaudhry, Sana, Shahlisa Hameedi, Junaid Altaf, Hafsa Gul, Nadia Bhutta, and Mehwish Sajjad. "Developmental Anomalies of Teeth – A cross-sectional study." Pakistan Journal of Medical and Health Sciences 15, no. 9 (2021): 2477–79. http://dx.doi.org/10.53350/pjmhs211592477.

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Background: This study was conducted to find out prevalence of tooth developmental anomalies and tooth agenesis syndrome in patients of Fariyal Dental College Lahore visiting the out-door department during the year 2017. Objective: The objective of this study was to conduct a retrospective examination of prevalence of developmental tooth anomalies and tooth agenesis syndrome .The relationship of age and gender was also focused. Methods: All patients of Fariyal Dental College Lahore visiting the out-patient department during the year 2017 were observed and analyzed. The documents scrutinized fo

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Wahyuni, Otty Ratna, Deny Saputra, Yunita Savitri, et al. "Distribution of dental anomalies in panoramic radiography at RSGMP Universitas Airlangga." Jurnal Radiologi Dentomaksilofasial Indonesia (JRDI) 8, no. 1 (2024): 1. http://dx.doi.org/10.32793/jrdi.v8i1.1133.

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Objectives: This research was aimed to determine the distribution of dental anomaly cases on panoramic radiographs at Universitas Airlangga Dental Hospital (RSGMP). Materials and Methods: This research used a descriptive observational design with a total sampling technique from panoramic radiographic data at the Radiology Clinic of RSGMP Universitas Airlangga during 2018–2020, which had cases of dental anomalies. Results: The result showed 116 cases of dental anomalies, with more incidence in female (64%) than in male (36%). The most common dental anomaly category was the number of teeth anoma

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Moca, Rahela Tabita, Abel Emanuel Moca, Raluca Iulia Juncar, Luminița Ligia Vaida, Anna-Maria Janosy, and Mihai Juncar. "Prevalence and Patterns of Positional Dental Anomalies in First Permanent Molars: Insights from a Study in Oradea, Romania." Diagnostics 14, no. 13 (2024): 1460. http://dx.doi.org/10.3390/diagnostics14131460.

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Tooth position anomalies, influenced by both genetic and environmental factors, can significantly impact oral health and play a critical role in establishing proper occlusion. The aim of this study was to identify the most prevalent tooth position anomalies in first permanent molars among Romanian patients and to evaluate additional variables as well. This retrospective study utilized digital study models to identify all existing tooth position anomalies. The study included patients aged 12 to 40 years with complete permanent dentition. Axial changes (buccal tilting, oral tilting, mesial tilti

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Bae, In-Hye, An-Na Choi, Sung-Ae Son, and Jeong-Kil Park. "Direct pulp capping and class II composite resin restoration of right maxillary first molar fused to supernumerary tooth." Journal of The Korean Dental Association 56, no. 6 (2018): 314–22. http://dx.doi.org/10.22974/jkda.2018.56.6.001.

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Among developmental anomalies of tooth shape, fusion and gemination are comparatively common. Developed with different etiologies, both fusion and gemination show similar clinical features. Therefore, many clinicians have difficulty diagnosing those morpho-anatomic anomalies. The purpose of this study is to report malformed right maxillary first molar in a 20-year-old female. With the aid of computed tomography (CT), the tooth was diagnosed as fusion with supernumerary tooth and dental caries lesion was detected. After performing direct pulp capping, the tooth was permanently restored with mic

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Aliev, Z. U. "Evaluation of attributable risk of dentoalveolar and facial anomalies prevalence among children depending on the features of family history." Kazan medical journal 98, no. 5 (2017): 701–3. http://dx.doi.org/10.17750/kmj2017-701.

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Aim. To assess the attributable risk of dentoalveolar and facial anomalies prevalence among children depending on the features of family history.  Methods. A sample of 2000 children was selected (250 boys and 250 girls from 4 age groups: 3-5, 6-9, 10-12 and 13-15 years). Characteristics of the family history was obtained by parents’ survey. The risk of dentoalveolar and facial anomalies was determined by comparing their frequency between groups with compromised and normal family history. Attributable risk was defined as the difference in the frequency of dentoalveolar and facial anomalie

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Camilleri, Simon. "Maxillary canine anomalies and tooth agenesis." European Journal of Orthodontics 27, no. 5 (2005): 450–56. http://dx.doi.org/10.1093/ejo/cji040.

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Alexander, Stanley A., Robert Serino, and Richard F. Ceen. "Deciduous tooth anomalies and partial anodontia." Oral Surgery, Oral Medicine, Oral Pathology 60, no. 2 (1985): 230. http://dx.doi.org/10.1016/0030-4220(85)90301-9.

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Gupta, Aakash, Arvinder Wander, Prakash Kumar, and Ramandeep Singh. "An Integrated Approach: Improving Tooth Nomenclature to Include Dental Abnormalities for Enhanced Clinical Diagnosis and Communication." Contemporary Clinical Dentistry 16, no. 1 (2025): 73–76. https://doi.org/10.4103/ccd.ccd_315_24.

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Abstract In dentistry, a tooth numbering system helps identify specific tooth positions in the mouth. This system includes quadrant types for primary and permanent teeth, making it easy to locate and document tooth positions. The tooth notation system is crucial for recording an individual’s case history and efficient clinical record keeping and standardizing diagnostic makeover. However, existing tooth charting systems lack the denotation of dental anomalies. To address this issue, we have introduced a modification in the commonly used tooth nomenclature (Zsigmondy Palmer system) to incorpora

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Rozprawy doktorskie na temat "Tooth Anomalies"

Maciel, Júlio César Córdova. "Avaliação da saúde bucal e anomalias dentárias em pacientes tratados com leucemia na infância e adolescência." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2005. http://hdl.handle.net/10183/6378.

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Objetivo: o objetivo deste estudo foi avaliar as condições de saúde bucal e a ocorrência de anomalias dentárias em crianças tratadas para leucemia linfoblástica aguda (LLA) no Serviço de Oncologia Pediátrica (SOP) do Hospital de Clínicas de Porto Alegre (HCPA), comparadas com um grupo crianças saudáveis. Amostra: foram selecionadas 56 crianças com diagnóstico de LLA e analisadas as presenças de anomalias dentárias e os índices CPO-D (cariado, perdido, obturado-dente), IPV (índice de placa visível), ISG (índice de sangramento gengival) e fluxo salivar. As crianças tratadas apresentaram uma médi

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Castro, Carlos Henrique Bettoni Cruz de. "Caracterização clínica, radiográfica e molecular da Síndrome de Van Der Woude." Universidade de São Paulo, 2006. http://www.teses.usp.br/teses/disponiveis/25/25136/tde-12062007-144801/.

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A Síndrome de Van der Woude (VWS) se caracteriza pela presença de fossetas congênitas no lábio inferior, associadas ou não à presença de fissura de lábio e/ou palato. Esta entidade é a forma sindrômica mais comum nos pacientes portadores de fissura labiopalatal, mesmo assim, ela é subdiagnosticada. Após o seqüenciamento do DNA, no ano de 2001, houve um aumento no interesse e no desenvolvimento de pesquisas na área de Genética Molecular Humana. Em 2002, pesquisadores identificaram no cromossomo 1, o gene IRF6 como sendo o responsável pela VWS. Neste trabalho, foram utilizados e analisados os pr

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Costa, Ana Maria Guerra. "Associação entre agenesia dentária e o padrão esquelético da face." Universidade de São Paulo, 2017. http://www.teses.usp.br/teses/disponiveis/58/58135/tde-01032018-144939/.

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O objetivo deste estudo foi avaliar a associação entre agenesia dentária e padrões esqueléticos faciais. A documentação ortodôntica inicial de 347 indivíduos foi avaliada para verificar a presença de agenesia dentária de pelo menos 1 dente permanente (excluindo terceiros molares) por meio de radiografias panorâmicas. Três medidas angulares foram avaliadas de cada radiografia cefalométrica (SNA, SNB e ANB). Os participantes do estudo foram agrupados em Classe I, Classe II e Classe III esquelética. Para a análise estatística, os indivíduos foram divididos em 2 grupos, \"com agenesia dentária\" e

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Morkmued, Supawich. "Approches cliniques, précliniques et translationnelles des anomalies bucco-dentaires associées aux maladies rares." Thesis, Strasbourg, 2017. http://www.theses.fr/2017STRAJ040.

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Les anomalies bucco-dentaires et crânio-faciales sont des manifestations phénotypiques des maladies rares. Ce doctorat combine les approches cliniques, précliniques et translationnelles en particulier par l’étude des modèles murins génétiquement modifiés reproduisant les maladies rares étudiées. Ce doctorat vise ainsi à identifier des gènes impliqués dans la morphogenèse et la signalisation inter-cellulaire en s’intéressant aux facteurs environnementaux et génétiques. Une étude détaille les effets d’un facteur d’environnement l’acide rétinoïque en excès sur du développement dentaire et la form

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Lopez, Diego Antonio Sigcho. "Anomalias dentárias e associações na fissura labiopalatina unilateral." Universidade de São Paulo, 2013. http://www.teses.usp.br/teses/disponiveis/61/61132/tde-03022014-085127/.

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Anomalias dentárias ocorrem com maior frequência em indivíduos com fissura labiopalatina (Slayton et al 2003) e em seus irmãos no afetados quando comparados à população sem fissura (Eerens et al 2001). Estudos realizados em indivíduos sem fissura demonstram que diferentes tipos de anomalias apresentam-se frequentemente associadas entre si (Baccetti 1998, Garib, Peck e Gomez 2009, Garib et al 2010). O objetivo do presente estudo foi determinar associações entre anomalias dentárias em indivíduos com fissura de lábio e palato, considerando que esse conhecimento pode fornecer informações essenciai

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Da, Cas Natália Ventura. "Prevalência de anomalias dentárias em pacientes portadores de fissuras labiopalatinas na região de Cascavel, PR." Universidade Estadual do Oeste do Paraná, 2017. http://tede.unioeste.br/handle/tede/3708.

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Submitted by Rosangela Silva (rosangela.silva3@unioeste.br) on 2018-05-28T14:28:16Z No. of bitstreams: 2 Natália Ventura da Cas.pdf: 886801 bytes, checksum: 85e6907201867651685baebab765b35d (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5)<br>Made available in DSpace on 2018-05-28T14:28:16Z (GMT). No. of bitstreams: 2 Natália Ventura da Cas.pdf: 886801 bytes, checksum: 85e6907201867651685baebab765b35d (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) Previous issue date: 2017-02-03<br>Coordenação de Aperfeiçoamento de Pessoal de Nível Sup

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Mori, Torres Estephany Cheril, and Chaña Nicole Andrea Diaz. "Asociación de la presencia de dientes en forma de pala y lesiones cariosas." Bachelor's thesis, Universidad Peruana de Ciencias Aplicadas (UPC), 2019. http://hdl.handle.net/10757/626308.

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Objetivo: Determinar la distribución entre el diente en forma de pala y la presencia de lesiones cariosas. Materiales y métodos: El presente estudio es de tipo transversal analítico. Se determinó un tamaño de muestra de 335 niños de 7 a 14 años de edad (1340 incisivos anterosuperiores) utilizando el Software EPIDAT, versión 4.2. Se consideró la clasificación de Hrdlička que se divide en no pala, trazo pala, semi pala y pala. Asimismo, se utilizó como instrumento el Sistema Internacional de Detección y Diagnóstico de Caries II (ICDAS II) para codificar la caries dental desde su estadio más te

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Planté-Bordeneuve, Violaine. "Neuropathies héréditaires par anomalie de la transthyrétine et des protéines myéliniques PMP22, P0 et de l'Egr2 : épidémiologie génétique et corrélations phénotype-génotype." Paris 11, 2001. http://www.theses.fr/2001PA11T044.

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Ce travail a étudié l'épidémiologie génétique de 61 familles françaises de neuropathies amyloides héréditaires (NAH), liées à la transthyrétine (TTR) et les corrélations phénotypegénotype de neuropathies sensitive-motrices démyélinisantes dominantes (formes de «Roussy-Lévy») et récessives dites de «Dejerine-Sottas» (DSS). Les familles de NAH réparties sur tout le territoire, incluent 12 mutations pathogènes hétérozygotes du gène de la TTR, dont Val30Met et Ser77Tyr (61% des familles) et 6 nouvelles substitutions (22% des familles). L'étude haplotypique montre la récurrence de Val30Met,Ser77Ph

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Monteiro, João Luís Salgado Ferreira Larcher. "Agenesias dentárias não-sindrómicas: genética associada." Master's thesis, 2019. http://hdl.handle.net/10284/7690.

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A agenesia dentária, ou hipodontia, é uma anomalia dentária caraterizada pela ausência de uma ou mais peças dentárias. Esta pode ter diversas causas e ocorre predominantemente na dentição permanente. O diagnóstico da agenesia dentária é efetuado por exame clínico e radiológico, enquanto a terapêutica deve ser adaptada a cada paciente. Com o presente trabalho procura-se esclarecer o conceito de agenesia dentária enquanto patologia e etiologia, na sua vertente sindrómica e não-sindrómica. Mais ainda, na vertente não-sindrómica, procura-se conhecer e avaliar os genes envolvidos. De forma a cump

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Casto, Carmelo Andrea. "Ortodontia: uma mais-valia em algumas síndromes e anomalias dentárias." Master's thesis, 2017. http://hdl.handle.net/10284/6378.

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Os dentes são um componente extremamente importante na cavidade oral. Ter órgãos dentários belos e saudáveis é sinónimo de uma boa higiene oral e a garantia de um sorriso invejável e sem complexos. A genética por vezes falha, podendo surgir anomalias dentárias e síndromes que afetam estes órgãos. Foi por esta razão que este trabalho despertou grande interesse, tendo como objetivo discutir algumas destas alterações, o que “correu mal” na formação, quais as características dessas alterações e como resolver o problema ortodonticamente. Sabe-se que a hipodontia, hiperdontia, microdontia e s

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Książki na temat "Tooth Anomalies"

Dentoorocraniofacial Anomalies And Genetics. Elsevier, 2012.

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Creigh, Peter D., and David N. Herrmann. Charcot-Marie-Tooth Disease and Pregnancy. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190667351.003.0025.

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Charcot-Marie-Tooth neuropathies (CMT) represent the most common hereditary neuropathies and can affect men and women from infancy to adulthood. There are no effective or FDA approved pharmacologic treatments aimed at disease modification for any form of CMT, so the primary focus of clinical care is on symptomatic treatment, maintaining functionality, and limiting secondary injury. CMT does not in general appear to affect a woman’s ability to carry a pregnancy. However, having CMT does increase the risk of delivery related complications (operative delivery, fetal presentation anomalies and pos

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Sybert, Virginia P. Disorders of Epidermal Appendages. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190276478.003.0003.

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Chapter 3 starts by covering conditions of the hair, including Alopecias (Loose Anagen Hair, Male Pattern Baldness, and Marie Unna Syndrome), Hirsutism (Gingival Fibromatosis and Hypertrichosis, Hypertrichosis Lanuginosa Congenita, Leprechaunism, and Localized Hypertrichosis), and Hair Shaft Abnormalities (including Monilethrix, Pili Annulati, Pili Torti, Pili Trianguli Et Canaliculi, Trichorrhexis Invaginata, Trichorrhexis Nodosa, Woolly Hair, Menkes Disease, Trichodentoosseous Syndrome, Trichorhinophalangeal Syndrome, and Trichothiodystrophy). It then covers conditions of the nails, includin

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Części książek na temat "Tooth Anomalies"

Soxman, Jane Ann, Patrice Barsamian Wunsch, and Christel M. Haberland. "Tooth Development." In Anomalies of the Developing Dentition. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-030-03164-0_1.

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Soxman, Jane Ann, Patrice Barsamian Wunsch, and Christel M. Haberland. "Anomalies of Tooth Number." In Anomalies of the Developing Dentition. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-030-03164-0_4.

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Soxman, Jane Ann, Patrice Barsamian Wunsch, and Christel M. Haberland. "Anomalies of Tooth Eruption." In Anomalies of the Developing Dentition. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-030-03164-0_5.

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Soxman, Jane Ann, Patrice Barsamian Wunsch, and Christel M. Haberland. "Anomalies of Tooth Formation." In Anomalies of the Developing Dentition. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-030-03164-0_6.

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Cooper, Lyndon F. "Treatment of Nonsyndromic Anomalies of Tooth Number." In Craniofacial and Dental Developmental Defects. Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-13057-6_4.

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Coil, Jeffrey M. "Radiographic Analysis of Anomalous Tooth Forms and Morphological Variations Related to Endodontics." In Endodontic Radiology. John Wiley & Sons, Ltd, 2017. http://dx.doi.org/10.1002/9781119421689.ch6.

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Litsas, George. "Dental Anomalies -Tooth Impaction." In Pediatric Orthodontics: Theory and Practice. BENTHAM SCIENCE PUBLISHERS, 2018. http://dx.doi.org/10.2174/9781681086095118020008.

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Parekh, S., and K. Harley. "Anomalies of tooth formation and eruption." In Paediatric Dentistry. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198789277.003.0022.

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Both the primary and permanent dentitions may be affected by variations in the number, size, and form of the teeth, as well as the structure of the dental hard tissues. These variations may be exclusively genetically determined, brought about by either local or systemically acting environmental factors, or possibly a combination of both genetic and environmental factors acting together. The same interplay of influences may affect the eruption and exfoliation of primary teeth, as well as the eruption of permanent teeth. This chapter considers a range of conditions involving abnormalities of the

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Bloch-Zupan, Agnès, Heddie O. Sedano, and Crispian Scully. "Abnormalities of Tooth Shape and Size." In Dento/Oro/Craniofacial Anomalies and Genetics. Elsevier, 2012. http://dx.doi.org/10.1016/b978-0-12-416038-5.00004-4.

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Severin, Emilia, George Gabriel Moldoveanu, and Andreea Moldoveanu. "Failure of Tooth Development: Prevalence, Genetic Causes and Clinical Features." In Human Teeth – Structure and Composition of Dental Hard Tissues and Developmental Dental Defects [Working Title]. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.99419.

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In dental practice may be encountered a wide variability in the clinical dental phenotype of tooth number. Failure of tooth development at the bud stage causes tooth agenesis and reduction in tooth number in the dental arch which involves various complications. Tooth agenesis is one of the most common developmental anomalies of human permanent dentition and tends to run in families, may aggregate within families, suggesting a genetic cause. Tooth agenesis can occur in association with a variety of craniofacial syndromes, but it is also found as an isolated trait (familial or sporadic). Other t

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