Results 81 to 90 of about 3,472 (237)
Dental Press Journal of Orthodontics, 2010 O presente trabalho versa sobre o diagnóstico e a abordagem ortodôntica das anomalias dentárias, enfatizando os aspectos etiológicos que definem tais irregularidades de desenvolvimento. Parece existir uma inter-relação genética na determinação de algumas
Daniela Gamba Garib +3 more
doaj +1 more source
Dental Treatment of Marfan Syndrome. With regard to a case. [PDF]
, 2010 Marfan syndrome is the most common dominant autosomic genetic disorder of the connective tissue. It has a reported incidence of 1 per each 5000 individuals without any distinction of gender or ethnicity.
Morales Chávez, Mariana Carolina +1 more
core +1 more source
Orthodontics &Craniofacial Research, Volume 29, Issue 2, Page 347-356, April 2026.ABSTRACT Objectives To investigate the influence of non‐syndromic hypodontia on radiographic dental development and to estimate dental age in children with bilateral mandibular agenesis using a machine learning approach. Materials and Methods This retrospective cross‐sectional study included 626 children aged 6–15 years (311 with dental agenesis, 315 ...
Marine Crosnier +3 more
wiley +1 more source
Defeito de desenvolvimento de esmalte em dente permanente resultante de entubação orotraqueal nos primeiros anos de vida [PDF]
RGO: Revista Gaúcha de OdontologiaRESUMO Os defeitos de desenvolvimento de esmalte são alterações resultantes de distúrbios no processo da amelogênese, podendo envolver fatores genéticos, sistêmicos, locais ou ambientais.
Raphaela Magalhães Coimbra +4 more
doaj +1 more source
American Journal of Medical Genetics Part A, Volume 200, Issue 3, Page 661-672, March 2026.ABSTRACT Noonan Syndrome (NS) is a clinically and genetically heterogeneous condition characterized by typical facial dysmorphisms, short stature, congenital heart defects, and developmental delays. While variants in genes such as PTPN11, SOS1, and RAF1 account for most genetically confirmed cases, diagnosis is challenging due to phenotypic overlap ...
Gabriela Jeesoo Kim +9 more
wiley +1 more source
Análisis mutacional del gen MSX1 en pacientes con FLPNS e hipodoncia
Revista Universitas Medica, 2009 Introducción. La etiología de la hendidura labio-palatina es compleja e involucra factores genéticos y ambientales. Además de la hendidura, numerosos estudios han reportado la presencia de anomalías dentales en asociación con varias formas de hendidura ...
SANDRA JANETH GUTIÉRREZ PRIETO +3 more
doaj
Oral findings in patients with Apert Syndrome Achados bucais em pacientes com Síndrome de Apert
Journal of Applied Oral Science, 2006 INTRODUCTION: The Apert syndrome is a rare disorder of autosomal dominant inheritance caused by mutations in the FGFR2 gene at locus 10q26; patients with this syndrome present severe syndactyly, exophthalmia, ocular hypertelorism and hypoplastic midface ...
Gisele da Silva Dalben +2 more
doaj +1 more source
Abordagem clínica de pacientes com síndrome de Down em medicina dentária [PDF]
, 2015 Projeto de Pós-Graduação/Dissertação apresentado à Universidade Fernando Pessoa como parte dos requisitos para obtenção do grau de Mestre em Medicina DentáriaO presente trabalho tem como objetivo a análise sobre a abordagem clinica de pacientes com ...
Silva, José Diogo Rodrigues da
core
Oral alterations and oral care in bone marrow transplant patients [PDF]
, 2008 Os cuidados gerais relativos ao paciente submetido ao transplante de medula óssea (TMO) incluem avaliações odontológicas rotineiras, as quais devem estar inseridas em um contexto multiprofissional.
BEZINELLI, Letícia M. +3 more
core +2 more sources
Health Science Reports, Volume 9, Issue 3, March 2026.ABSTRACT Background and Aim As dental anomalies can significantly affect esthetic and function, early detection and diagnosis are crucial for treatment and minimizing potential negative effects. Artificial intelligence (AI) has emerged as a promising tool for the segmentation and detection of dental anomalies in number, morphology, size, position, and ...
Mobina Sadat Zarabadi +4 more
wiley +1 more source