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[PMID]:29068927
[Au] Autor:Veeramani A; Sawh R; Steinbacher DM
[Ad] Endereço:New Haven, Conn. From Yale Plastic Surgery.
[Ti] Título:Orthognathic Surgery and Rhinoplasty to Address Nasomaxillary Hypoplasia.
[So] Source:Plast Reconstr Surg;140(5):930-932, 2017 Nov.
[Is] ISSN:1529-4242
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:The treatment of nasomaxillary hypoplasia is challenging. The phenotype of Binder "syndrome" includes the following: midfacial hypoplasia, class III malocclusion, small or absent anterior nasal spine, flattened nose, horizontal nostrils, short columella, acute nasolabial angle, and a flat frontonasal angle. A staged approach is used, with orthognathic surgery to achieve vertical maxillary length and sagittal advancement, followed by rhinoplasty aimed to increase nasal tip projection, rotation, and columellar length. This article details the diagnosis and treatment of nasomaxillary hypoplasia, demonstrating the senior author's (D.M.S.) preferred approach and technical steps. CLINICAL QUESTION/LEVEL OF EVIDENCE: Therapeutic, V.
[Mh] Termos MeSH primário: Anormalidades Maxilofaciais/cirurgia
Procedimentos Cirúrgicos Ortognáticos/métodos
Rinoplastia/métodos
[Mh] Termos MeSH secundário: Adolescente
Feminino
Seres Humanos
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE; VIDEO-AUDIO MEDIA
[Em] Mês de entrada:1711
[Cu] Atualização por classe:171109
[Lr] Data última revisão:
171109
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:171026
[St] Status:MEDLINE
[do] DOI:10.1097/PRS.0000000000003789


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[PMID]:28964289
[Au] Autor:Fu Y; Li C; Dai P; Zhang T
[Ad] Endereço:ENT Institute, Eye & ENT Hospital of Fudan University, Shanghai 200031, China.
[Ti] Título:Three-dimensional assessment of the temporal bone and mandible deformations in patients with congenital aural atresia.
[So] Source:Int J Pediatr Otorhinolaryngol;101:164-166, 2017 Oct.
[Is] ISSN:1872-8464
[Cp] País de publicação:Ireland
[La] Idioma:eng
[Ab] Resumo:OBJECTIVE: To investigate the deformations of temporal bone and mandible combined with congenital aural atresia. METHODS: A total of 158 patients with congenital aural atresia were included in the study. The raw CT data of the temporal bone was imported into MIMICS v 12 and threshold dissection, region growing and three-dimensional (3D) calculation were used to calculate 3D models. The 3D characteristics of the temporal bone and upper part of mandible were assessed. RESULTS: The tympanic part of the temporal bone was all undeveloped. Of all the patients included, 14 patients were found to have severe maxillofacial malformations. Among them, 2 cases have floating arch, 4 cases have interrupted arch, 5 cases have mandibular processes hypoplasia and 3 cases have interrupted arch combined with severe maxillary malformation. Ten of the 14 patients were suffered from dysplasia of the mastoid part of the temporal bone as well. CONCLUSION: Maxillofacial malformations may sometimes coexist with congenital aural atresia. Otolaryngologists should not neglect the coexisted maxillofacial malformations and give timely referral to maxillofacial surgeons.
[Mh] Termos MeSH primário: Anormalidades Congênitas/diagnóstico por imagem
Orelha/anormalidades
Imagem Tridimensional/métodos
Mandíbula/anormalidades
Osso Temporal/anormalidades
Tomografia Computadorizada por Raios X/métodos
[Mh] Termos MeSH secundário: Dissecação
Orelha/diagnóstico por imagem
Feminino
Seres Humanos
Masculino
Mandíbula/diagnóstico por imagem
Anormalidades Maxilofaciais/complicações
Anormalidades Maxilofaciais/epidemiologia
Osso Temporal/diagnóstico por imagem
Adulto Jovem
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1710
[Cu] Atualização por classe:171023
[Lr] Data última revisão:
171023
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:171002
[St] Status:MEDLINE


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[PMID]:28841625
[Au] Autor:Doumit G; Totonchi A; Wexler A; Gosain AK
[Ad] Endereço:Montreal, Quebec, Canada; Cleveland, Ohio; Los Angeles, Calif.; Chicago, Ill. From the Division of Plastic Surgery, University of Montreal; the Division of Plastic Surgery, Metro Hospital; the Division of Plastic Surgery, Kaiser Permanente Medical Center; and the Division of Plastic Surgery, Lurie Children's Hospital of Northwestern Feinberg School of Medicine.
[Ti] Título:American Society of Maxillofacial Surgeons 2006 to 2016: Another Decade of Excellence in Education and Research.
[So] Source:Plast Reconstr Surg;140(3):487e-494e, 2017 Sep.
[Is] ISSN:1529-4242
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Over the past 10 years, the American Society of Maxillofacial Surgeons (ASMS) has continued to advance to meet its mission of being the premier organization to represent maxillofacial and pediatric plastic surgery in the United States. These advances are focused on education of its members, to include the American Society of Maxillofacial Surgeons basic course, the preconference symposium, the annual meeting, two basic maxillofacial courses per year, advanced maxillofacial courses, a boot camp for craniofacial fellows, a cleft course, quarterly webinars, sponsored fellowships, a visiting professorship, and the ASMS journal. In addition, the ASMS has continued to advance as the premier national organization representing maxillofacial and pediatric plastic surgery in the United States, thereby positioning the organization as a primary advocate for these surgical specialties. Outreach of the ASMS has grown over the past decade and now includes representatives to the American Society of Plastic Surgeons/Plastic Surgery Foundation, the American Board of Plastic Surgeons, the American Medical Association, and most recently a seat as a governor with the American College of Surgeons. The ASMS has also initiated an annual Summer Leadership Seminar to explore topics of relevance in a changing health care environment. The present report outlines the major initiatives of the ASMS over the past 10 years.
[Mh] Termos MeSH primário: Anormalidades Maxilofaciais/cirurgia
Traumatismos Maxilofaciais/cirurgia
Sociedades Médicas
Cirurgia Plástica
[Mh] Termos MeSH secundário: Pesquisa Biomédica
Seres Humanos
Cirurgia Plástica/educação
Estados Unidos
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1709
[Cu] Atualização por classe:170918
[Lr] Data última revisão:
170918
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:170826
[St] Status:MEDLINE
[do] DOI:10.1097/PRS.0000000000003599


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[PMID]:28791817
[Au] Autor:Drozdowski PH; Latkowski I; Zachara MG; Wójcicki P
[Ad] Endereço:Plastic Surgery Unit, Specialist Medical Centre, Polanica Zdrój, Poland.
[Ti] Título:Binder syndrome: Clinical findings and surgical treatment of 18 patients at the Department of Plastic Surgery in Polanica Zdrój.
[So] Source:Adv Clin Exp Med;26(3):427-437, 2017 May-Jun.
[Is] ISSN:1899-5276
[Cp] País de publicação:Poland
[La] Idioma:eng
[Ab] Resumo:BACKGROUND: Binder syndrome (BS) is an uncommon congenital underdevelopment of the maxilla and nasal skeleton. Other clinical features include a hypoplastic or absent anterior nasal spine; a short, flat nose with short columella; an acute nasolabial angle; a convex upper lip and class III malocclusion. OBJECTIVES: The aim of the study was to outline the major characteristics of BS and to present a variety of surgical treatment methods. MATERIAL AND METHODS: The study included 18 patients treated in the authors' department from 1989 to 2013. RESULTS: The patients were predominantly women, aged 6 months to 34 years. Nine patients did not present any co-morbidities, but in the other 9 the most common co-morbidities were a unilateral cleft lip and palate, followed by a cleft palate, a bilateral cleft lip and palate, a cleft lip, GERD, gluten intolerance, oligophrenia, goiter and foot malformation. Most of the patients had not been operated on previously. The most common procedure carried out was an iliac crest bone graft. In 4 patients, no procedures other than cleft lip and palate repair were undertaken. In 3 cases a Le Fort I osteotomy was performed to correct the patients' orthognathic status. No major or life-threating complications were noted. In 2 cases, due to a high degree of resorption of bone grafts, multiple secondary grafting of bone, cartilage and deepithelialized skin was necessary to obtain satisfactory results. CONCLUSIONS: In BS surgical treatment is the treatment of choice. It results in adequate correction of facial retrusion. However, due to various degrees of bone resorption, the results are not lifelong. No unequivocally superior surgical strategy in BS has been presented so far. Most disagreement among authors is related to the need for and timing of maxillary osteotomy, the choice between bone and cartilage grafting in nose reconstruction and columella lengthening. Although alloplastic materials offer the tempting advantage of fast and simultaneous augmentation of deficient tissues, their use may risk prolonged infections and extrusion, resulting in exacerbations of deformities.
[Mh] Termos MeSH primário: Anormalidades Maxilofaciais/cirurgia
[Mh] Termos MeSH secundário: Adolescente
Adulto
Transplante Ósseo/métodos
Criança
Pré-Escolar
Fenda Labial/cirurgia
Fissura Palatina/cirurgia
Feminino
Seres Humanos
Lactente
Masculino
Má Oclusão de Angle Classe III/cirurgia
Maxila/cirurgia
Nariz/anormalidades
Osteotomia de Le Fort/métodos
Procedimentos Cirúrgicos Reconstrutivos/métodos
Cirurgia Plástica/métodos
Adulto Jovem
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1710
[Cu] Atualização por classe:171004
[Lr] Data última revisão:
171004
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170810
[St] Status:MEDLINE
[do] DOI:10.17219/acem/62123


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[PMID]:28705589
[Au] Autor:Wei J; Luo J; Herrler T; Xu H; Deng N; Li Q; Dai C
[Ad] Endereço:Department of Plastic and Reconstructive Surgery, Shanghai Jiaotong University Medical School, Ninth People's Hospital, China.
[Ti] Título:A simple technique for the correction of maxillonasal dysplasia using customized expanded polytetrafluoroethylene (ePTFE) implants.
[So] Source:J Plast Reconstr Aesthet Surg;70(9):1292-1297, 2017 Sep.
[Is] ISSN:1878-0539
[Cp] País de publicação:Netherlands
[La] Idioma:eng
[Ab] Resumo:BACKGROUND: The treatment of maxillonasal dysplasia in Binder's syndrome using autologous costal bone and cartilage is well established, but postoperative results may be compromised by scarring, unpredictable absorption of transferred autologous tissue, and donor site morbidity. Here, we propose a simple surgical technique to improve maxillonasal dysplasia using an expanded polytetrafluoroethylene (ePTFE) implant. MATERIALS AND METHODS: From February 1999 to May 2014, fifty-eight patients affected by maxillonasal dysplasia with different degrees of flattened nose and midfacial depression underwent surgical correction by augmentation of the nasal dorsum using an "L"-shaped ePTFE and subperiosteal implantation of an inverted "m"-shaped ePTFE at the base of the piriform aperture. The outcome was evaluated based on preoperative and postoperative patient pictures, 3D imaging technology for the assessment of nasolabial angle and facial convexity angle, and a postoperative patient satisfaction survey. RESULTS: Postoperative results showed improved facial aesthetics with a significantly increased nasolabial angle from initially 74.1° ± 8.9° to 93.7° ± 6.1° at 6 months postoperatively (p < 0.05). Temporary discomfort involving upper lip numbness, foreign body sensation, and stiff smiling expression were complained during the first 3 months postoperatively, but spontaneously resolved within 6 months. Complications included infection (2 cases), implant migration (2 cases), and implant exposure (1 case). The vast majority of patients (95.7%) rated their postoperative outcome as highly improved and improved. CONCLUSION: The present therapeutic strategy provides a simple and effective treatment for the correction of maxillonasal dysplasia with high patient acceptance in a single step approach. Further research is required to determine long-term outcomes.
[Mh] Termos MeSH primário: Anormalidades Maxilofaciais/cirurgia
Politetrafluoretileno
Próteses e Implantes
Procedimentos Cirúrgicos Reconstrutivos/métodos
[Mh] Termos MeSH secundário: Adolescente
Adulto
Feminino
Seres Humanos
Masculino
Meia-Idade
Fatores de Tempo
Resultado do Tratamento
Adulto Jovem
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
9002-84-0 (Polytetrafluoroethylene)
[Em] Mês de entrada:1709
[Cu] Atualização por classe:170914
[Lr] Data última revisão:
170914
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170715
[St] Status:MEDLINE


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[PMID]:28319315
[Au] Autor:Cohen N; Cohen E; Gaiero A; Zecca S; Fichera G; Baldi F; Giordanetto JF; Mercier JM; Cohen A
[Ad] Endereço:Department of Pediatric and Neonatology, Inter-Regional Center for Rare-Diseases, San Paolo Hospital, Savona, Italy.
[Ti] Título:Maxillofacial features and systemic malformations in expanded spectrum Hemifacial Microsomia.
[So] Source:Am J Med Genet A;173(5):1208-1218, 2017 May.
[Is] ISSN:1552-4833
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Hemifacial microsomia (HFM) is a rare, multisystemic congenital disease with estimated frequency of 1/26370 births in Europe. Most cases are sporadic and caused by unilateral abnormal morphogenesis of the first and second pharyngeal arches. The aim of this study is to define the types and frequency of maxillofacial and systemic malformations in HFM patients. This is a case series study of patients with HFM evaluated at a single institution. Data were acquired through history, physical examination, photographs, diagnostic radiology, and laboratory and analyzed by the FileMakerPro database on 95 patients (54F; 41M) of which 89 met the inclusion criteria. Mandibular hypoplasia was observed in 86 patients with right-side preponderance (50). One patient had bilateral mandibular hypoplasia. Seventy-four had external ear anomalies (anotia or microtia). Eleven had bilateral malformed ears. Hearing impairment, associated with stenosis or atresia of the external ear canal, was found in 69 patients (eight with bilateral canal defects). Ocular anomalies were seen in 41 (23 with dermoid cysts) and 39 had orbital malformations. Facial nerve paralysis was observed in 38 patients. Cleft lip/palate (10), preauricular tags (55), and macrostomia (41) were also described. A total of 73/86 had systemic malformations, mainly vertebral (40), genitourinary (25), and cardiovascular (28). Sixteen had cerebral anomalies (four with intellectual disability). All patients suspected of HFM should undergo a complete systematic clinical and imaging investigation to define the full scope of anomalies. Since the disease is rare and complex, affected patients should be monitored by specialized multidisciplinary team centers.
[Mh] Termos MeSH primário: Fenda Labial/genética
Assimetria Facial/genética
Síndrome de Goldenhar/genética
Anormalidades Maxilofaciais/genética
[Mh] Termos MeSH secundário: Anormalidades Múltiplas/diagnóstico
Anormalidades Múltiplas/genética
Adolescente
Criança
Pré-Escolar
Fenda Labial/diagnóstico
Fenda Labial/fisiopatologia
Fissura Palatina/diagnóstico
Fissura Palatina/genética
Fissura Palatina/fisiopatologia
Orelha Externa/anormalidades
Assimetria Facial/diagnóstico
Assimetria Facial/fisiopatologia
Feminino
Síndrome de Goldenhar/diagnóstico
Síndrome de Goldenhar/fisiopatologia
Seres Humanos
Lactente
Masculino
Mandíbula/anormalidades
Anormalidades Maxilofaciais/diagnóstico
Anormalidades Maxilofaciais/fisiopatologia
Meia-Idade
Adulto Jovem
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1705
[Cu] Atualização por classe:170508
[Lr] Data última revisão:
170508
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170321
[St] Status:MEDLINE
[do] DOI:10.1002/ajmg.a.38151


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[PMID]:28292696
[Au] Autor:Santinoni CD; Oliveira HF; Batista VE; Lemos CA; Verri FR
[Ad] Endereço:Dental School, Univ. Estadual Paulista - UNESP, Araçatuba, Brazil; Dental School, Univ. do Oeste Paulista - UNOESTE, Presidente Prudente, Brazil.
[Ti] Título:Influence of low-level laser therapy on the healing of human bone maxillofacial defects: A systematic review.
[So] Source:J Photochem Photobiol B;169:83-89, 2017 Apr.
[Is] ISSN:1873-2682
[Cp] País de publicação:Switzerland
[La] Idioma:eng
[Ab] Resumo:PURPOSE: This systematic review evaluates the effectiveness of low-level laser therapy (LLLT) to enhance maxillofacial area bone repair. METHODS: A comprehensive search of studies published up to February 2017 and listed in PubMed/MEDLINE, Scopus, and Cochrane Library databases was performed in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement. RESULTS: The 15 selected studies evaluated a total of 374 patients (mean age, 28.5years) who were treated with LLLT. Gallium-arsenide (GaAs) and gallium aluminium arsenide (GaAlAs) were the most commonly used devices, and LLLT parameters varied greatly. Wavelengths varied from 500 to 1000nm. Tooth extraction, distraction osteogenesis, maxillary expansion, periodontal defects, orthodontic movement and maxillary cystic defects were evaluated. From the 15 selected studies, six evaluated bone repair (primary outcomes). Of these, four studies showed improvement in bone formation after using LLLT, two demonstrated improved results for only one follow up period, and one showed no additional benefits. The other 9 studies evaluated secondary parameters related to healing (secondary outcomes) in the maxillofacial area after applying LLLT, including anti-inflammatory, analgesic, and healing accelerator effects, and quality of life related to oral health. There were no adverse or negative effects of LLLT reported. CONCLUSION: Within the limitation of this review, a possible improvement in bone density can be found when LLLT is applied postoperatively in maxillofacial bony defects. LLLT also seems to promote anti-inflammatory and analgesic effects and accelerate healing, as well as enhance quality of life related to oral health. However, LLLT use protocols need to be standardized before more specific conclusions can be drawn about this subject.
[Mh] Termos MeSH primário: Terapia com Luz de Baixa Intensidade/métodos
Anormalidades Maxilofaciais/terapia
Traumatismos Maxilofaciais/terapia
[Mh] Termos MeSH secundário: Adulto
Seres Humanos
Anormalidades Maxilofaciais/patologia
Traumatismos Maxilofaciais/patologia
Osteogênese
Cicatrização
[Pt] Tipo de publicação:JOURNAL ARTICLE; META-ANALYSIS; REVIEW
[Em] Mês de entrada:1704
[Cu] Atualização por classe:170426
[Lr] Data última revisão:
170426
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170316
[St] Status:MEDLINE


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[PMID]:27540624
[Au] Autor:Dmytriw AA; Song JS; Power S; Saliou G; terBrugge K
[Ad] Endereço:1 Department of Medical Imaging, University of Toronto, Toronto, ON, Canada.
[Ti] Título:Management of a large diffuse maxillofacial arteriovenous malformation previously treated with ligation of ipsilateral arterial supply.
[So] Source:Dentomaxillofac Radiol;46(1):20160130, 2017 Jan.
[Is] ISSN:0250-832X
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:A 32 year-old male presented with a pulsatile facial mass with palpable thrill and audible bruit. Imaging revealed a very large diffuse left-sided facial arteriovenous malformation with extensive bilateral supply, as well as a previously ligated left external carotid artery. Endovascular treatment was required to control associated hemorrhagic events as well as for palliation and was delivered via the contralateral and ipsilateral collateral supply because of ligation of the direct route to the nidus. In addition, the patient received intravenous bevacizumab and intraarterial bleomycin therapy. Under such circumstances, endovascular embolization remains often the only option when emergent therapy for massive haemorrhage is required. Collaboration and treatment planning with head and neck surgery is imperative and should be performed from the onset, avoiding disastrous ligation of arterial feeders.
[Mh] Termos MeSH primário: Malformações Arteriovenosas/diagnóstico por imagem
Malformações Arteriovenosas/terapia
Face/irrigação sanguínea
Face/diagnóstico por imagem
Anormalidades Maxilofaciais/diagnóstico por imagem
Anormalidades Maxilofaciais/terapia
[Mh] Termos MeSH secundário: Adulto
Inibidores da Angiogênese/uso terapêutico
Antibióticos Antineoplásicos/uso terapêutico
Bevacizumab/uso terapêutico
Bleomicina/uso terapêutico
Terapia Combinada
Progressão da Doença
Drenagem
Embolização Terapêutica
Evolução Fatal
Seres Humanos
Ligadura
Masculino
Extração Dentária
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Angiogenesis Inhibitors); 0 (Antibiotics, Antineoplastic); 11056-06-7 (Bleomycin); 2S9ZZM9Q9V (Bevacizumab)
[Em] Mês de entrada:1703
[Cu] Atualização por classe:170924
[Lr] Data última revisão:
170924
[Sb] Subgrupo de revista:D
[Da] Data de entrada para processamento:160820
[St] Status:MEDLINE


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[PMID]:27534905
[Au] Autor:Kakutani H; Sato Y; Tsukamoto-Takakusagi Y; Saito F; Oyama A; Iida J
[Ad] Endereço:Clinical Department of Orthodontics, Hokkaido University Hospital, Sapporo, Japan.
[Ti] Título:Evaluation of the maxillofacial morphological characteristics of Apert syndrome infants.
[So] Source:Congenit Anom (Kyoto);57(1):15-23, 2017 Jan.
[Is] ISSN:1741-4520
[Cp] País de publicação:Australia
[La] Idioma:eng
[Ab] Resumo:Apert syndrome is a rare craniosynostosis syndrome characterized by irregular craniosynostosis, midface hypoplasia, and syndactyly of the hands and feet. Previous studies analyzed individuals with Apert syndrome and reported some facial and intraoral features caused by severe maxillary hypoplasia. However, these studies were performed by analyzing both individuals who had and those had not received a palate repair surgery, which had a high impact on the maxillary growth and occlusion. To highlight the intrinsic facial and intraoral features of Apert syndrome, five Japanese individuals with Apert syndrome from 5 years and 2 months to 9 years and 10 months without cleft palate were analyzed in this study. A concave profile and a skeletal Class III jaw-base relationship caused by severe maxillary hypoplasia were seen in all patients. The patients exhibited anterior and posterior crossbites possibly due to a small dental arch of Maxilla.
[Mh] Termos MeSH primário: Acrocefalossindactilia/diagnóstico
Anormalidades Maxilofaciais/diagnóstico
Fenótipo
[Mh] Termos MeSH secundário: Acrocefalossindactilia/cirurgia
Pré-Escolar
Arco Dental/anormalidades
Facies
Feminino
Seres Humanos
Lactente
Masculino
Anormalidades Maxilofaciais/cirurgia
Radiografia
Anormalidades Dentárias
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1702
[Cu] Atualização por classe:170206
[Lr] Data última revisão:
170206
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:160819
[St] Status:MEDLINE
[do] DOI:10.1111/cga.12180


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[PMID]:28005777
[Au] Autor:Pipalia H; Ganesh P; Shetty S; Salins PC; Raut R; Boyina KK
[Ad] Endereço:Department of Craniofacial Surgery, Mazumdar Shaw Cancer Centre, Bangalore, India.
[Ti] Título:Virtual Surgery Planning in Orthomorphic Correction of Mandibular Dysmorphology.
[So] Source:J Craniofac Surg;27(8):2156-2158, 2016 Nov.
[Is] ISSN:1536-3732
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Three-dimensional virtual surgery programs are widely available for orthognathic surgery. The advent of imaging software programs has proved to be useful for diagnosis, treatment planning, outcome measurement, and three-dimensional surgical simulation. Complex maxillofacial malformations continue to present challenges in analysis and correction beyond modern technology. Orthomorphic correction for mandibular dysmorphology refers to basal bone movement without any change in dental component. The purpose of this paper is to present a virtual surgery planning for surgeons to perform the orthomorphic surgery with precision and quantification. Moreover, it provides an essential educational tool for patients to foresee predicted surgical outcome.
[Mh] Termos MeSH primário: Simulação por Computador
Imagem Tridimensional/métodos
Mandíbula/cirurgia
Anormalidades Maxilofaciais/cirurgia
Procedimentos Cirúrgicos Ortognáticos/métodos
Cirurgia Assistida por Computador/métodos
Interface Usuário-Computador
[Mh] Termos MeSH secundário: Feminino
Seres Humanos
Mandíbula/diagnóstico por imagem
Anormalidades Maxilofaciais/diagnóstico
Adulto Jovem
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1703
[Cu] Atualização por classe:170817
[Lr] Data última revisão:
170817
[Sb] Subgrupo de revista:D
[Da] Data de entrada para processamento:161223
[St] Status:MEDLINE
[do] DOI:10.1097/SCS.0000000000003117



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BIREME/OPAS/OMS - Centro Latino-Americano e do Caribe de Informação em Ciências da Saúde