Mandibular Prognathism
Mostrando 1-12 de 18 artigos, teses e dissertações.
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1. Craniofacial geometric morphometrics in the identification of patients with sickle cell anemia and sickle cell trait
ABSTRACT Objective: The aims of this study were to identify the main characteristics regarding the shape and size of the craniofacial region in patients with sickle cell anemia (SCA) and sickle cell trait (SCT) and in unaffected patients using geometric morphometrics and to check the efficiency of this method. Material and Methods: A cross-sectional analyt
Hematol., Transfus. Cell Ther.. Publicado em: 2020-10
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2. Skeletal Class III malocclusion treatment using mandibular and maxillary skeletal anchorage and intermaxillary elastics: a case report
RESUMO Introdução: a Classe III esquelética é considerada uma das más oclusões mais difíceis de se tratar. Em cerca de 40% dos pacientes afligidos por ela, a principal causa do problema é o retrognatismo maxilar e, na maioria desses pacientes, o tratamento ortopédico/cirúrgico inclui algum tipo de protração da maxila. Objetivo: o objetivo do
Dental Press J. Orthod.. Publicado em: 11/11/2019
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3. Relationship between skeletal Class II and Class III malocclusions with vertical skeletal pattern
RESUMO Objetivo: o objetivo do presente estudo foi estabelecer a relação entre os padrões esqueléticos sagitais e verticais, e avaliar quais variáveis esqueléticas podem influenciar na chance de desenvolver uma má oclusão de Classe II ou de Classe III esquelética. Métodos: foi feito um estudo transversal, cuja amostra incluiu radiografias cefalo
Dental Press J. Orthod.. Publicado em: 05/09/2019
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4. Class III malocclusion with maxillary deficiency, mandibular prognathism and facial asymmetry
RESUMO Este artigo relata o caso clínico de uma paciente do sexo feminino, com história de insucessos em tratamentos ortodônticos pregressos. Apresentava má oclusão de Classe III, com atresia de ambas as arcadas dentárias, mordida cruzada anterior e assimetria facial, proveniente de laterognatismo desencadeado por uma hiperatividade condilar, manifesta
Dental Press J. Orthod.. Publicado em: 2016-12
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5. Severe Angle Class III skeletal malocclusion associated to mandibular prognathism: orthodontic-surgical treatment
RESUMO O presente caso clínico descreve o tratamento ortodôntico de um paciente com 18 anos e 1 mês de idade, portador de má oclusão esquelética de Classe III, com prognatismo mandibular e significativa compensação dentária. A relação entre caninos era de Classe III, incisivos com tendência à mordida cruzada e mordida aberta, moderado apinhament
Dental Press J. Orthod.. Publicado em: 2016-12
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6. Fragile X syndrome: panoramic radiographic evaluation of dental anomalies, dental mineralization stage, and mandibular angle
ABSTRACT Fragile X syndrome (FXS) is a disorder linked to the chromosome X long arm (Xq27.3), which is identified by a constriction named fragile site. It determines various changes, such as behavioral or emotional problems, learning difficulties, and intellectual disabilities. Craniofacial abnormalities such as elongated and narrow face, prominent forehead,
J. Appl. Oral Sci.. Publicado em: 2016-10
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7. Cephalometric characteristics of Class III malocclusion In Brazilian individuals
Aim: To evaluate the cephalometric characteristics of Class III malocclusion in Caucasian Brazilian subjects. Methods: The sample comprised 71 lateral cephalograms of individuals not previously submitted to any orthodontic treatment. The Class III group (experimental group) comprised 37 patients with bilateral Class III molar relationship and ANB lower than
Braz. J. Oral Sci.. Publicado em: 2014-12
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8. Cephalometric evaluation of pharyngeal airway space changes in class III patients undergoing orthognathic surgery : retrospective study / Avaliação cefalométrica das alterações da via aérea superior em pacientes classe III submetidos à cirurgia ortognática : estudo retrospectivo
The configuration and dimensions of the upper airway are determined by the anatomical structures such as soft tissue, muscles and craniofacial skeleton, which comprise or surround the pharynx. Anatomic abnormalities of the soft tissue and/or the craniofacial skeleton may narrow the upper airway leading to obstructive sleep apnea. Class III patients, after or
Publicado em: 2010
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9. Deglutição: estudo eletromiográfico da atividade dos músculos masseter, temporal e digástrico. / Swallowing: an electomyographic study of the activity of the masseter, temporal and digastric muscles.
Abstract In order to study the electromyographic activity of the masseter, temporal anterior and digastric in swallowing with and without dental occlusion, we evaluated 43 women, aged between 19 and 34 years (mean 23 years), students from the Undergraduate or Graduate Department of Speech Therapy of the Federal University of São Paulo. All had permanent tee
Publicado em: 2010
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10. Relação anatomica entre a morfologia cranio-facial, o espaço aereo faringeo, a posição do osso hioide e a postura cranio-cervical / Anatomical relation between the craniofacial morphology, pharyngeal airway space, the hyoid bone position and the craniocervical posture
The aim of this research was to evaluate the relation between the craniofacial morphology, pharyngeal airway space, the hyoid bone position and the craniocervical posture. Lateral cephalometric radiographs were obtained from 52 volunteers in natural head posture, among 18 and 28 years old, of both genders, randomly selected, that had not historical of orthod
Publicado em: 2009
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11. Genética do prognatismo mandibular: avaliação de heredogramas, análise complexa de segregação e análise de ligação com loci candidatos em famílias brasileiras averiguadas a partir de probandos afetados
There is a familial tendency to mandibular prognathism. Various genetic models have been described. It is assumed to be a polygenic trait in the vast majority of cases, with a threshold for expression. The purpose of the current study was to examine specific genetic models of the familial transmission of MP in Brazilian families and to search for evidences o
Publicado em: 2006
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12. Phonoaudiological aspects of Saethre-Chotzen syndrome / Aspectos fonoaudiologicos da sindrome de Saethre-Chotzen
Saethre-Chotzen Syndrome (SCS) is characterized by craniosynostosis and several important facial alterations such as: low hair implantation at the front, asymmetry, maxillary hypoplasia, mandibular prognathism, in addition to small, dysmorphic and low-set ears. Among the ocular alterations are: blepharoptosis, strabismus, epicanthus, lachrymal duct stenosis
Publicado em: 2006