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1.
Glycobiology ; 34(5)2024 Apr 19.
Artigo em Inglês | MEDLINE | ID: mdl-38438145

RESUMO

This review delves into the roles of glycosaminoglycans (GAGs), integral components of proteoglycans, in tooth development. Proteoglycans consist of a core protein linked to GAG chains, comprised of repeating disaccharide units. GAGs are classified into several types, such as hyaluronic acid, heparan sulfate, chondroitin sulfate, dermatan sulfate, and keratan sulfate. Functioning as critical macromolecular components within the dental basement membrane, these GAGs facilitate cell adhesion and aggregation, and play key roles in regulating cell proliferation and differentiation, thereby significantly influencing tooth morphogenesis. Notably, our recent research has identified the hyaluronan-degrading enzyme Transmembrane protein 2 (Tmem2) and we have conducted functional analyses using mouse models. These studies have unveiled the essential role of Tmem2-mediated hyaluronan degradation and its involvement in hyaluronan-mediated cell adhesion during tooth formation. This review provides a comprehensive summary of the current understanding of GAG functions in tooth development, integrating insights from recent research, and discusses future directions in this field.


Assuntos
Glicosaminoglicanos , Ácido Hialurônico , Camundongos , Animais , Glicosaminoglicanos/metabolismo , Proteoglicanas/metabolismo , Sulfato de Queratano/metabolismo , Sulfatos de Condroitina/metabolismo , Heparitina Sulfato/metabolismo , Odontogênese , Dermatan Sulfato
2.
Eur J Orthod ; 46(1)2024 Jan 01.
Artigo em Inglês | MEDLINE | ID: mdl-37847809

RESUMO

BACKGROUND: Masticatory activity affects the morphology of the maxillo-mandibular complex, however, its influence on the cranial base remains to be elucidated. The recent integration of quantitative morphometric analysis with 3D imaging enabled a comprehensive and high-resolution morphological characterization of the craniofacial complex. We aimed to investigate the influence of masticatory activity on the morphology of the growing cranial base by three-dimensional (3D) geometric morphometric approach using micro-CT. METHODS: The micro-CT data was reanalyzed to illustrate the 3D shape of the cranial base, and wireframe models were generated by connecting landmarks on the images. In the original study, mice were fed a soft diet (SD) of powdered pellets or a conventional hard diet (HD) for 6 weeks from 3 to 9 weeks of age, immediately after weaning. A principal component (PC) analysis analyzed shape variations and assessed their significance, while canonical variate (CV) analysis facilitated the comparison and differentiation of groups based on shape, unveiling meaningful shape distinctions. RESULTS: Three PCs were extracted that significantly separated the SD and HD groups among those explaining variations in shape. These PCs were related to the length of the sphenoid bone, the width of the anterior part of the sphenoid bone, and the length of the cranial base. Furthermore, one CV effectively distinguished SD from HD, and CV analysis showed that the sphenoid was shortened in the length and narrowed at the border of the temporal bone in SD mice. CONCLUSIONS: Masticatory loading affects the skeletal development of the cranial base. The morphology of the sphenoid bone was affected in both the sagittal and transverse axes.


Assuntos
Mandíbula , Base do Crânio , Camundongos , Animais , Base do Crânio/diagnóstico por imagem , Mandíbula/diagnóstico por imagem , Microtomografia por Raio-X , Dieta , Imageamento Tridimensional
3.
Am J Med Genet A ; 191(7): 1984-1989, 2023 07.
Artigo em Inglês | MEDLINE | ID: mdl-37141439

RESUMO

Craniofacial defects are one of the most frequent phenotypes in syndromic diseases. More than 30% of syndromic diseases are associated with craniofacial defects, which are important for the precise diagnosis of systemic diseases. Special AT-rich sequence-binding protein 2 (SATB2)-associated syndrome (SAS) is a rare syndromic disease associated with a wide variety of phenotypes, including intellectual disability and craniofacial defects. Among them, dental anomalies are the most frequently observed phenotype and thus becomes an important diagnostic criterion for SAS. In this report, we demonstrate three Japanese cases of genetically diagnosed SAS with detailed craniofacial phenotypes. The cases showed multiple dental problems, which have been previously reported to be linked to SAS, including abnormal crown morphologies and pulp stones. One case showed a characteristic enamel pearl at the root furcation. These phenotypes add new insights for differentiating SAS from other disorders.


Assuntos
Deficiência Intelectual , Proteínas de Ligação à Região de Interação com a Matriz , Humanos , População do Leste Asiático , Síndrome , Fenótipo , Deficiência Intelectual/diagnóstico , Deficiência Intelectual/genética , Proteínas de Ligação à Região de Interação com a Matriz/genética , Fatores de Transcrição/genética
4.
Cleft Palate Craniofac J ; 60(12): 1556-1564, 2023 12.
Artigo em Inglês | MEDLINE | ID: mdl-35748725

RESUMO

To determine dental and palatal morphology in children with cleft lip and/or palate (CL/P) and identify morphological prognostic factors for orthognathic surgery (OGS).Retrospective cohort study.Orthodontic department of a university dental hospital.This study included 80 patients with bilateral and unilateral CL/P who had lateral cephalograms at the ages of 7 (T1), 15 (T2) years, and a dental plaster model at T1.Plaster models at T1 were scanned with a three-dimensional (3D) scanner. Morphological features were extracted from 3D models with geometric morphometrics software as principal components (PCs). The combinations of the PCs and other predictive factors (ie, the No. of clefts in the lip and alveolus, the palatal repair method, sex, cephalometric variables at T1, and the No. of missing teeth) were examined by logistic regression to determine the predictability for OGS. The need for OGS and skeletal and dental discrepancies at T2 were examined as outcomes.Shrinkage of the palate, including vertical shallowing and transverse narrowing of the posterior maxilla and cleft-side asymmetry of the anterior maxilla at T1, as well as the No. of clefts in the lip and alveolus, the palatal repair method, male sex, several cephalometric variables for the sagittal and vertical dimensions, and the No. of missing teeth, were found to be predictive factors for OGS.Morphological prognostic factors for OGS in children with CL/P were determined.


Assuntos
Fenda Labial , Fissura Palatina , Cirurgia Ortognática , Humanos , Masculino , Criança , Fenda Labial/diagnóstico por imagem , Fenda Labial/cirurgia , Fissura Palatina/diagnóstico por imagem , Fissura Palatina/cirurgia , Estudos Retrospectivos , Prognóstico , Dentição , Maxila/diagnóstico por imagem , Maxila/cirurgia , Cefalometria
5.
Cleft Palate Craniofac J ; : 10556656231201834, 2023 Sep 21.
Artigo em Inglês | MEDLINE | ID: mdl-37735913

RESUMO

Sotos syndrome is a genetic disorder characterized by distinct craniofacial features, overgrowth in childhood, and impaired intellectual development. We herein report the successful orthodontic treatment of a 14-year-old boy with Sotos syndrome caused by a heterozygous mutation in the NSD1 gene. He showed severe hypodontia, impaction of the maxillary second molars and a skeletal Class III jaw-base relationship. Orthodontic management, including space control by protraction of the maxillary first molars and traction of the impacted molars, was performed using fixed appliances and miniscrews. As a result, acceptable occlusion was obtained without any discernible relapse 18 months postretention.

6.
Am J Orthod Dentofacial Orthop ; 163(4): e93-e105, 2023 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-36621352

RESUMO

INTRODUCTION: The morphology of the human face varies broadly, with genetic and environmental factors determining these variations. Examining variations in the 3-dimensional (3D) craniomandibular morphology and identifying related factors (eg, sex differences) are important in orthodontic clinics. This study observed shape variations in the 3D facial morphology of Japanese adults showing skeletal Class 1 malocclusion and examined the association of sexual dimorphism with shape variations. METHODS: Sixty cone-beam computed tomography images of Japanese adults (30 males and 30 females) with skeletal Class I malocclusion were employed. In each cone-beam computed tomography image, wire mesh fitting was conducted as previously described. A principal component (PC) analysis after Procrustes registration and the PC clustering method was conducted to observe the shape variations. A PC regression analysis was conducted to determine the sexual morphologic characteristics. RESULTS: Nine PCs depicting 62% of the morphology were determined. Four typical phenotypes were found, mainly related to mandibular protrusion (PC1) and the vertical divergence of the face (PC2). PCs related to sex determination were PC3 (robustness of the mandibular angle in males), PC5 (greater size and shape of the coronoid and mastoid processes in males), and PC7 (greater maxillary width in males), accounting for 16% of total variations. CONCLUSIONS: The major shape variations in skeletal Class 1 subjects were related to nonsexual dimorphic characteristics (ie, mandibular protrusion and facial divergence). Sexual dimorphic characteristics were evaluated in detail and accounted for 16% of total morphologic variations.


Assuntos
Má Oclusão Classe I de Angle , Caracteres Sexuais , Humanos , Adulto , Masculino , Feminino , População do Leste Asiático , Cefalometria/métodos , Mandíbula/diagnóstico por imagem , Mandíbula/anatomia & histologia , Tomografia Computadorizada de Feixe Cônico
7.
Curr Osteoporos Rep ; 20(1): 120-126, 2022 02.
Artigo em Inglês | MEDLINE | ID: mdl-34931296

RESUMO

PURPOSE OF REVIEW: The Runx family genes (Runx1, Runx2, Runx3, and Cbfb) are important transcriptional regulators in the development of various tissues. We herein highlight the roles of the Runx family genes in morphogenesis in the craniofacial regions and in the pathogenesis of congenital morphological problems in these regions. RECENT FINDINGS: A recent analysis using conditional Runx mutant animals and a human genetic study identified the novel roles of Runx genes in the development of the tooth, salivary glands, and the palate. In an animal study, Runx1/Cbfb signaling was found to regulate the Lgr5 expression and maintain the stem cells in the dental epithelium in the growing incisors. Aberrant Runx1/Cbfb signaling induced male-specific involution of the convoluted granular cell differentiation of the submandibular gland. In palatogenesis, Runx1/Cbfb signaling regulated the Tgfb3 expression in the fusing palatal epithelium through Stat3 activation. The combination of a human genetic study and a phenotype analysis of mutant animals revealed the various roles of Runx genes in the development of the tooth, palate, and salivary glands. Runx genes have functional redundancy in various tissues, which still hinder the roles of Runx genes in morphogenesis. Future studies may reveal the novel roles of Runx signaling.


Assuntos
Subunidade alfa 2 de Fator de Ligação ao Core , Transdução de Sinais , Animais , Osso e Ossos/metabolismo , Subunidade alfa 2 de Fator de Ligação ao Core/genética , Subunidade alfa 2 de Fator de Ligação ao Core/metabolismo , Humanos , Masculino , Fenótipo , Transdução de Sinais/genética
8.
Orthod Craniofac Res ; 25(3): 351-358, 2022 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-34606173

RESUMO

OBJECTIVE: The purpose of this study was to evaluate the errors of three-dimensional mandibular surfaces generated using magnetic resonance imaging (MRI) when computed tomography (CT) was set as the gold standard. SETTINGS AND SAMPLE POPULATION: Seven patients with orthognathic deformities who had undergone CT and MRI scans were included in the study. MATERIALS AND METHODS: Mandibular surfaces were generated on each CT and MR image by the surface-rendering method. Intra-individual reliability between CT and MRI was statistically tested by the confidence limits of agreement (LOA) for systematic error, 95% confidence interval minimal detectable change (MDC95 ) for random error and intra-class correlation coefficient (ICC). RESULTS: The average total error was 1.6 mm. The greatest MDC95 was observed in the coronoid region in all directions. The other regions showed MDC95 values of < 1.8 mm (transvers direction), 3.5 mm (vertical direction) and 1.7 mm (antero-posterior direction). ICCs showed 'almost perfect' agreement with respect to all regions. CONCLUSION: Random errors were quantified for 3-D rendering of the mandible from MRI data. Although the coronoid region showed the greatest errors, the other regions of the mandibular surfaces generated using MRI were able to be evaluated.


Assuntos
Imageamento Tridimensional , Tomografia Computadorizada por Raios X , Humanos , Imageamento Tridimensional/métodos , Imageamento por Ressonância Magnética/métodos , Mandíbula/diagnóstico por imagem , Reprodutibilidade dos Testes , Tomografia Computadorizada por Raios X/métodos
9.
J Esthet Restor Dent ; 34(4): 583-591, 2022 06.
Artigo em Inglês | MEDLINE | ID: mdl-35182447

RESUMO

OBJECTIVE: This case report describes the orthodontic and prosthetic rehabilitation of a patient with resorption of the roots of the maxillary central incisors due to the ectopic maxillary canines. CLINICAL CONSIDERATIONS: A 16-year-old woman presented with severe resorption of the roots of the maxillary central incisors due to the ectopic maxillary canines. The impacted canines were orthodontically tracted with a lingual arch-supporting temporary central incisors and vertical elastics, and, undesirable root proximity was later corrected by moving the canines distally 1.5 mm apart. Gingival replacement cords were placed into the gingival sulcus of the canines, and tooth preparation was performed along with rotary gingival curettage of the interdental papilla. Convex form was provided for the mesial and labio-distal subgingival contour of the restorations. CONCLUSIONS: The creeping attachment of the interdental papilla was successfully achieved by the orthodontic arrangement of interdental distance and the prosthetic stimulus via the retraction cord, rotary curettage, and convex mesial subgingival contours. In addition, selective retraction of the labio-distal gingiva by overcontoured restorations moved the gingival zenith position (GZP) distally. Finally, the canine crown morphology and gingival level mimicked the central incisors. CLINICAL SIGNIFICANCE: This clinical report introduces a treatment workflow of to recover the esthetic disturbance due to severe root resorption of the maxillary central incisors associated with impacted maxillary canines. The present orthodontic and prosthetic procedure can improve both hard and soft tissue esthetics and could be used in similar cases, such as malformed teeth and tooth autotransplantation or transposition with disturbances in the interdental papilla height or the GZP.


Assuntos
Reabsorção da Raiz , Dente Impactado , Adolescente , Dente Canino , Humanos , Incisivo/anatomia & histologia , Maxila , Reabsorção da Raiz/terapia , Dente Impactado/complicações , Dente Impactado/terapia
10.
Am J Orthod Dentofacial Orthop ; 161(4): 542-547, 2022 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-34629236

RESUMO

INTRODUCTION: The use of aligner therapy for orthodontic treatment has increased substantially in the past decade. However, no study has compared treatment outcomes between the conventional fixed appliance and Invisalign therapies in patients with a severe deep overbite. METHODS: This study included 50 consecutive adult patients who underwent treatment with either Invisalign (n = 25; mean age, 23.3 ± 8.5 years) or a conventional fixed appliance (n = 25; mean age, 23.1 ± 6.5 years) to correct overbite >5 mm and >60% deep overbite. Cephalometric analysis and peer assessment rating was used to compare the clinical outcome between groups. RESULTS: Cephalometric analysis showed significant differences in N-Me (P = 0.0005) and Mp-L6 (P = 0.0001) between Invisalign and fixed appliance treatment groups. No significant differences were observed in the peer assessment rating analysis or total treatment duration between the 2 groups. CONCLUSIONS: Both Invisalign and conventional fixed appliances were effective in treating patients with a severe deep overbite. Invisalign therapy may be preferable over conventional fixed appliance therapy in patients with high angle and deep overbite. However, because this study had a retrospective design, the results should be viewed with caution.


Assuntos
Aparelhos Ortodônticos Removíveis , Sobremordida , Adolescente , Adulto , Cefalometria , Humanos , Desenho de Aparelho Ortodôntico , Aparelhos Ortodônticos Fixos , Sobremordida/terapia , Estudos Retrospectivos , Adulto Jovem
11.
Eur J Orthod ; 44(4): 436-444, 2022 08 16.
Artigo em Inglês | MEDLINE | ID: mdl-35050343

RESUMO

AIM: This study was aimed to evaluate two artificial intelligence (AI) systems that created a prioritized problem list and treatment plan, and examine whether the performance of the aforementioned systems was equivalent to orthodontists. MATERIALS AND METHODS: A total of 967 consecutive cases [800: training; 67: validation; 100: evaluation (40: randomly selected for the clinical evaluation)] were used. We used a stored document that describes (1) the patient's clinical information, (2) the prioritized list, and (3) a treatment strategy without digital tooth movement. Sentences of (1) were vectorized according to the bag of words method (V); sentences of (2) and (3) were relabelled with 423 and 330 labels, respectively. AI systems that output labels for the prioritized list (subtask 1) and treatment planning (subtask 2) based on the vectors V were developed using a support vector machine and self-attention network, respectively, while the system was trained to improve precision and recall. Clinical evaluations were conducted by four orthodontists (no faculty or residents; peer group) in two sessions: in the first session, peer group and the developed AI systems created problem lists and treatment plans; in the second session, two of the peer group (not AI) evaluated these lists and plans, including the lists and plans of the AIs, by scoring them using 4-point scales [unacceptable (1) to ideal (4)]. Scores were compared among the system and peer group (Wilcoxon signed-rank test, P < 0.05). RESULTS: The precision after system training was 65% and 48% for subtasks 1 and 2 respectively, with recall of 55% and 48%, respectively. The clinical evaluation of the AI system for subtask 1 showed a mid-rank. For subtask 2, the AI system had a significantly lower score than the three panels but the same rank with one panel. CONCLUSIONS: Two AI systems that output a prioritized problem list and create a treatment plan were developed. The clinical system ability of the former system showed a mid-rank in the peer group, and the latter system was almost equivalent to the worst orthodontist.


Assuntos
Inteligência Artificial , Técnicas de Movimentação Dentária , Humanos
12.
Orthod Craniofac Res ; 24 Suppl 2: 153-162, 2021 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-33599070

RESUMO

OBJECTIVE: To determine the prognostic factors for orthognathic surgery (OGS) in children with cleft lip and/or palate (CL/P) using artificial intelligence (AI) systems. DESIGN: Retrospective cohort study. SETTING: An orthodontic department at a university dental hospital. PARTICIPANTS: This study included 126 patients with bilateral and unilateral CL/P for whom lateral cephalograms were obtained at three time points: 7 (T1), 10 (T2) and 15 (T3) years of age. MAIN OUTCOME MEASURES: Cleft type, severity of lip separation at birth, number of missing teeth, sex, palatal repair methods and surgeons, cephalometric variables at T1 and T2, and the total duration of orthodontic treatment were examined as predictors. The need for OGS and skeletal and dental discrepancies at T3 was examined as outcomes. RESULTS: A total of six models were developed, with a mean area under the receiver operating characteristic curve of 0.93. Multiple prognostic factors for OGS were identified. In particular, the number of clefts in the lip and alveolus showed relatively high odds ratios, as did anterior crossbite at T3. Achieving palatal closure with the push-back method, rather than Furlow's method, was also found to be a predictive factor for anterior crossbite at T3, with high odds ratios. CONCLUSIONS: The prognostic factors for OGS determined by the AI systems were the number of clefts in the lip and alveolus, the palatal repair method, male sex, several cephalometric variables for the sagittal and vertical dimensions, growth patterns and the number of missing teeth.


Assuntos
Fenda Labial , Fissura Palatina , Cirurgia Ortognática , Inteligência Artificial , Criança , Fenda Labial/cirurgia , Fissura Palatina/cirurgia , Humanos , Recém-Nascido , Masculino , Prognóstico , Estudos Retrospectivos
13.
Orthod Craniofac Res ; 24 Suppl 2: 43-52, 2021 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-34021976

RESUMO

OBJECTIVES: To determine whether AI systems that recognize cephalometric landmarks can apply to various patient groups and to examine the patient-related factors associated with identification errors. SETTING AND SAMPLE POPULATION: The present retrospective cohort study analysed digital lateral cephalograms obtained from 1785 Japanese orthodontic patients. Patients were categorized into eight subgroups according to dental age, cleft lip and/or palate, orthodontic appliance use and overjet. MATERIALS AND METHODS: An AI system that automatically recognizes anatomic landmarks on lateral cephalograms was used. Thirty cephalograms in each subgroup were randomly selected and used to test the system's performance. The remaining cephalograms were used for system learning. The success rates in landmark recognition were evaluated using confidence ellipses with α = 0.99 for each landmark. The selection of test samples, learning of the system and evaluation of the system were repeated five times for each subgroup. The mean success rate and identification error were calculated. Factors associated with identification errors were examined using a multiple linear regression model. RESULTS: The success rate and error varied among subgroups, ranging from 85% to 91% and 1.32 mm to 1.50 mm, respectively. Cleft lip and/or palate was found to be a factor associated with greater identification errors, whereas dental age, orthodontic appliances and overjet were not significant factors (all, P < .05). CONCLUSION: Artificial intelligence systems that recognize cephalometric landmarks could be applied to various patient groups. Patient-oriented errors were found in patients with cleft lip and/or palate.


Assuntos
Fenda Labial , Fissura Palatina , Inteligência Artificial , Cefalometria , Fenda Labial/diagnóstico por imagem , Fissura Palatina/diagnóstico por imagem , Humanos , Estudos Retrospectivos
14.
Acta Med Okayama ; 75(2): 205-212, 2021 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-33953427

RESUMO

We herein report the case of a 19-year-old female with a transverse discrepancy, skeletal Class II malocclusion, severe crowding with concerns of classic-type Ehlers-Danlos syndrome (EDS), aesthetics problems and functional problems. The main characteristics of classic EDS are loose-jointedness and fragile, easily bruised skin that heals with peculiar "cigarette-paper" scars. The anteroposterior and transverse skeletal discrepancies can generally be resolved by maxilla repositioning and mandibular advancement surgery following pre-surgical orthodontic treatment. However, this patient was treated with orthodontic camouflage but not orthognathic surgery because of the risks of skin bruising, poor healing and a temporomandibular disorder. A satisfactory dental appearance and occlusion were achieved after camouflage treatment with orthodontic anchor screws and the use of Class II elastics, including the preservation of the stomatognathic functions. Acceptable occlusion and dentition were maintained after a two-year retention period. This treatment strategy of orthodontic camouflage using temporary anchorage, such as anchor screws and Class II elastics, may be a viable treatment option for skeletal malocclusion patients with EDS.


Assuntos
Síndrome de Ehlers-Danlos/complicações , Má Oclusão Classe II de Angle/terapia , Procedimentos de Ancoragem Ortodôntica/métodos , Feminino , Humanos , Qualidade de Vida , Adulto Jovem
15.
Cleft Palate Craniofac J ; 58(11): 1459-1467, 2021 11.
Artigo em Inglês | MEDLINE | ID: mdl-33272028

RESUMO

Prader-Willi syndrome (PWS) is a rare genetic disorder caused by a defect in paternally expressed genes in the 15q11-q13 region. Prader-Willi syndrome affects many parts of the body and involves craniofacial and dentofacial abnormalities. We herein report the successful 2-stage orthodontic treatment of an 8-year-old girl with PWS caused by paternal 15q11-q13 deletion. She presented with a skeletal class II relationship with mandibular deviation, a deep overbite, and severe crowding of the lower dental arch. Functional appliance therapy was utilized to improve her skeletal discrepancy. The second phase of orthodontic treatment using fixed appliances was started at 14.5 years old, which improved her remained crowding and large overbite. As a result, her facial appearance and occlusion were improved without any discernible relapse after 2 years of retention. We describe the outcomes of orthodontic treatment for a patient with PWS and discuss the specific attention during orthodontic treatment.


Assuntos
Má Oclusão Classe II de Angle , Síndrome de Prader-Willi , Adolescente , Criança , Oclusão Dentária , Feminino , Humanos , Aparelhos Ortodônticos Fixos , Síndrome de Prader-Willi/terapia , Doenças Raras
16.
Cleft Palate Craniofac J ; 57(2): 255-262, 2020 02.
Artigo em Inglês | MEDLINE | ID: mdl-31382775

RESUMO

Basal cell nevus syndrome (BCNS) is a rare genetic disorder that can be caused by mutation of multiple genes, including PTCH1, PTCH2, and SUFU, in an autosomal dominant manner. The symptoms include some craniofacial features such as keratocystic odontogenic tumors (KCOTs), macrocephaly, and cleft lip and/or palate. Although comprehensive orthodontic treatment is frequently required for some of these craniofacial deformities, there are few reports that show the outcomes of comprehensive orthodontic treatment. Here, we report a case of BCNS with multiple KCOTs, macrocephaly, skeletal class III malocclusion, asymmetric dental arch, and mandibular crowding, which was successfully treated with comprehensive orthodontic treatment.


Assuntos
Síndrome do Nevo Basocelular , Fenda Labial , Má Oclusão , Tumores Odontogênicos , Humanos , Mutação
17.
Am J Orthod Dentofacial Orthop ; 158(4): 535-546, 2020 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-32826124

RESUMO

INTRODUCTION: The purpose of this study was to apply a previously reported homologous model for quantifying and visualizing the three-dimensional (3D) cranio-mandibular morphology. METHODS: Twenty-eight 3D cone-beam computed tomography (CBCT) images of Japanese patients (7 to 13 years of age) showing skeletal Class 1 malocclusions were used in this study. Wire mesh fitting was conducted for each patient based on the assignment of landmarks to each 3D surface (homologous modeling). Cranial and mandibular images were generated using surface rendering of the CBCT images. The mean and standard deviation of each point on the wire mesh were calculated as the normative mean. Two operators conducted the process twice for seven patients, with a one-week interval between fittings. The intra- and inter-examiner reliability were determined using the 95% confidence interval minimal detectable change (MDC95) for random error and intra-class correlation coefficients (ICCs). RESULTS: The intra- and inter-examiner reliability of the mesh fitting method were almost perfect. Normative ranges of the cranial and mandibular surfaces of Japanese were determined. CONCLUSIONS: A clinical method that enables practitioners to quantify and visualize the hard tissues of a patient's face in three dimensions with almost perfect reliability is presented. This method allows practitioners to evaluate how patients' skeletal characteristics differ from normative means in three dimensions.


Assuntos
Imageamento Tridimensional , Mandíbula/diagnóstico por imagem , Adolescente , Cefalometria , Criança , Tomografia Computadorizada de Feixe Cônico , Humanos , Reprodutibilidade dos Testes
18.
Eur J Orthod ; 42(5): 509-516, 2020 11 03.
Artigo em Inglês | MEDLINE | ID: mdl-32346737

RESUMO

BACKGROUND AND OBJECTIVES: The masticatory force affects craniofacial development. We aimed to quantify the topological deviation of the growing craniofacial structure due to soft-food diet feeding and to map the region where the phenotypes appeared on three-dimensional (3D) images. MATERIAL AND METHODS: Mice were fed a powdered soft diet (SD) or conventional hard diet (HD) of regular rodent pellets at 3 weeks of age until 9 weeks of age. The heads, excluding the mandibles, were scanned by micro-computed tomography. The topographic deviation of the bony surface was quantitatively assessed by a wire mesh fitting analysis. The actual displacement and significant differences were mapped and visualized in each x-, y-, and z-axis on the 3D craniofacial image. On these reconstructed images, two-dimensional linear measurements between the landmark points confirmed the 3D skeletal displacement. RESULTS: In the transverse direction, the zygomatic arches and the region in which the temporal muscle attaches to the parietal and temporal bones were narrow in the SD group. The temporal muscle attachment regions significantly shifted anteriorly, and consequently, the sagittal zygomatic arch shortened. Although the cranial sagittal length was not affected, the vertical height was also reduced in the SD group compared to the HD group. CONCLUSIONS: Our 3D surface-based analysis demonstrated that SD feeding resulted in reduced 3D bony development at the region where the chewing muscles attach to the zygomatic arches and the temporal and parietal bones. Interestingly, SD feeding induced an anterior shift in the temporal and parietal bone regions, which can affect the skeletal inter-jaw relationship.


Assuntos
Mastigação , Zigoma , Animais , Dieta , Imageamento Tridimensional , Mandíbula , Camundongos , Microtomografia por Raio-X , Zigoma/diagnóstico por imagem
19.
Cleft Palate Craniofac J ; 56(3): 400-407, 2019 03.
Artigo em Inglês | MEDLINE | ID: mdl-29787302

RESUMO

Orthodontic treatment in patients with orofacial cleft such as cleft lip and palate or isolated cleft palate is challenging, especially when the patients exhibit severe maxillary growth retardation. To correct this deficiency, maxillary expansion and protraction can be performed in the first phase of orthodontic treatment. However, in some cases, the malocclusion cannot be corrected by these procedures, and thus, skeletal discrepancy remains when the patients are adolescents. These remaining problems occasionally require various orthognathic treatments according to the degree of the discrepancy. Here, we describe one case of a female with isolated cleft palate and hand malformation who exhibited severe maxillary deficiency until her adolescence and was treated with multiple orthognathic surgeries, including surgically assisted maxillary expansion (surgically assisted rapid palatal expansion), LeFort I osteotomy, and bilateral sagittal split osteotomy in order to correct severe skeletal discrepancy and malocclusion. The treatment resulted in balanced facial appearance and mutually protected occlusion with good stability. The purpose of this case report is to show the orthodontic treatment outcome of 1 patient who exhibited isolated cleft palate and subsequent severe skeletal deformities and malocclusion which was treated by an orthodontic-surgical approach.


Assuntos
Fenda Labial , Fissura Palatina , Má Oclusão Classe III de Angle , Má Oclusão , Adolescente , Feminino , Humanos , Maxila , Técnica de Expansão Palatina
20.
Cleft Palate Craniofac J ; 56(7): 978-985, 2019 08.
Artigo em Inglês | MEDLINE | ID: mdl-30626201

RESUMO

OBJECTIVE: This report describes the case of a male patient with a complete unilateral cleft lip and palate who presented with midface deficiency and an anteroposteriorly constricted maxilla. DESIGN: Case report Interventions: Correction involved anterior distraction of the segmented maxilla. RESULTS: The present case demonstrates that elongation of the maxilla with anterior distraction is an effective way to develop a proper dental arch, correct anterior and posterior crowding, and improve a midface deficiency.


Assuntos
Fenda Labial , Fissura Palatina , Arco Dental , Má Oclusão , Osteogênese por Distração , Fenda Labial/cirurgia , Fissura Palatina/cirurgia , Arco Dental/crescimento & desenvolvimento , Humanos , Masculino , Maxila
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