Academic literature on the topic 'Mandible, abnormalities'

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Journal articles on the topic "Mandible, abnormalities"

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Tongol, Erik A., Alfredo Q. Y. Pontejos, Phillip B. Fullante, Arsenio Claro A. Cabungcal, and Kimberly Mae C. Ong. "Intraosseus Arteriovenous Malformation of the Mandible: Extracorporeal Curettage and Immediate Replantation." Philippine Journal of Otolaryngology-Head and Neck Surgery 34, no. 1 (2019): 56–59. http://dx.doi.org/10.32412/pjohns.v34i1.969.

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Objective: To describe a surgical technique in the treatment of arteriovenous malformations of the mandible
 Methods:
 Design: Case Report
 Setting: Tertiary National University Hospital
 Participants: One
 Result: A 16-year-old boy underwent resection, extracorporeal curettage, and immediate replantation of the hemimandible for intraosseous arteriovenous malformation. Postoperative follow up and imaging at one- and six-months showed no signs of recurrence, new bone formation and consolidation of the replanted right mandible with good symmetry and function.
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Inokuchi, Mikiko, Jouji Nomura, Yoshihiko Mtsumura, Motoko Sekida, and Toshiro Tagawa. "Sotos syndrome with enamel hypoplasia: a case report." Journal of Clinical Pediatric Dentistry 25, no. 4 (2001): 313–16. http://dx.doi.org/10.17796/jcpd.25.4.n52851t26173843u.

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A rare case of Sotos syndrome with enamel hypoplasia is described. Dental abnormalities include enamel hypoplasia, expansion of the pulp cavity, high arched palate, and absence of the bilateral premolar teeth of the mandible.
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Bouletreau, Pierre, and Christian Paulus. "Surgical correction of transverse skeletal abnormalities in the maxilla and mandible." International Orthodontics 10, no. 3 (2012): 261–73. http://dx.doi.org/10.1016/j.ortho.2012.06.007.

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Ekberg, O., I. Redlund-Johnell, and K. G. Sjöblom. "Pharyngeal Function in Patients with Rheumatoid Arthritis of the Cervical Spine and Temporomandibular Joint." Acta Radiologica 28, no. 1 (1987): 35–39. http://dx.doi.org/10.1177/028418518702800107.

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Pharyngeal function was studied in 31 patients with rheumatoid arthritis. Eighteen of these patients had dysphagia. Cervical spine abnormalities were present in 14. Destruction of the capitulum and/or ramus of the mandible was registered in 9. Pharyngeal dysfunction was revealed in 20. Patients with a vertical dislocation of the C1–C2 in relation to the occipital bone and patients with destruction of the capitulum and/or ramus of the mandible had an increased frequency of pharyngeal dysfunction. Pharyngeal dysfunction is thought to be due to mechanical factors and caused by derangements of mus
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Zhang, Beibei, Xiaoyun Pan, Dandan Chi, et al. "Arhgap29 Deficiency Directly Leads to Systemic and Craniofacial Skeletal Abnormalities." International Journal of Molecular Sciences 26, no. 10 (2025): 4647. https://doi.org/10.3390/ijms26104647.

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The Arhgap29 gene encodes Rho-GTPase-activating protein 29 (Arhgap29), which plays a crucial role in embryonic tissue development. Mutations in the Arhgap29 gene are significantly associated with non-syndromic cleft lip and palate (NSCL/P). Our study demonstrated that the deletion of Arhgap29 leads to syndromic cleft lip and palate (SCL/P) characteristics in mice, where, in addition to cleft palate, the mice exhibit craniofacial and systemic skeletal abnormalities. However, the mechanisms underlying these skeletal abnormalities remain unclear. Through micro-CT imaging, histological analysis, a
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PAPAGEORGIOU, OURANIA, DIMITRIS A. PAPANASTASIOU, NICHOLAS G. BERATIS, PANAGIOTIS KOROVESSIS та ALEKOS OIKONOMOPOULOS. "Scoliosis in β Thalassemia". Pediatrics 88, № 2 (1991): 341–45. http://dx.doi.org/10.1542/peds.88.2.341.

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Skeletal abnormalities in patients with homozygous β thalassemia have been noted as early as 1927 by Cooley et al1 and have been the subject of many reviews.2-5 Abnormalities have been observed in the entire skeletal system, especially the skull and the mandible, giving the patients a characteristic appearance. Bone changes cause mainly expansion of the medullary cavity, subperiosteal overgrowth of the bones of the skull, and cortical thinning with porous rarefaction of the long bones. Although most of the bone abnormalities in inadequately transfused thalassemic patients result from the overg
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Puspitaningtyas, Dyah Ayu, Alfian Danie, and Muhammad Fa’ik. "Effectiveness of Head MSCT Examination in Cases of Mild Head Injuries." Journal of Health (JoH) 12, no. 1 (2025): 119–25. https://doi.org/10.30590/joh.v12n1.900.

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Mild Head Injury (MIH) with a Glasgow Coma Scale (GCS) score of 13-15, has symptoms of temporary loss of neurological function, mild to severe headache and vomiting, CT-Scan examination is performed if there are signs of skull fracture and vomiting more than once. MSCT examination of the head at the Radiology of Salatiga City Hospital uses a scan area from the vertex to the mandible. The purpose of this study was to determine the effectiveness of Head MSCT examination in mild head injury cases. The research method used was descriptive qualitative method with a case study approach. The study wa
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RA, Noorul, Suganya S, Murugesan K, and Muthukumar B. "Alternative Prosthodontic Management Of Segmental Mandibulectomy - A Case Report." JOURNAL OF CLINICAL PROSTHODONTICS AND IMPLANTOLOGY 1, no. 1 (2019): 7–10. http://dx.doi.org/10.55995/j-cpi.2019002.

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Ameloblastoma is a benign tumor of odontogenic epithelial origin commonly affecting the mandible than the maxilla. The ameloblastoma is a rare metastatic neoplasm with lesions causing abnormalities of face and jaw. Abnormal cell growth would affect the surrounding bony structures which could be managed only by surgical excision. Mandibulectomy of various levels could be done depending on the extent of the lesion. Surgical excision of mandible can be done with or without preservation of the basal cortical bone. Prosthodontic management of mandibulectomy patients with alternate options than conv
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Manor, Esther, Sarit Tetro, Monica Noyhous, Palina Kachko, and Lipa Bodner. "Translocation (2;13) and other chromosome abnormalities in intraosseous schwannoma of the mandible." Cancer Genetics and Cytogenetics 193, no. 2 (2009): 116–18. http://dx.doi.org/10.1016/j.cancergencyto.2009.04.022.

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Chen, Wendy, Jack Brooker, Joshua Barnett, et al. "Pediatric Mandibular Distraction Osteogenesis and Long-Term Dental Morbidity: A Clinical Evaluation and Review of the Literature." FACE 2, no. 3 (2021): 275–80. http://dx.doi.org/10.1177/27325016211026331.

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Objectives: Pediatric mandibular distraction osteogenesis (MDO) is an increasingly common surgical procedure used to lengthen the mandible. Little is known about the long-term effects of MDO on dental development. This retrospective study sought to identify dental abnormalities at mixed dentition and early permanent dentition stages in patients who had undergone MDO. Methods: All pediatric patients who underwent MDO with imaging and clinical exams at mixed dentition and early permanent dentition stages were evaluated identify pathology. Data included demographic information, medical and surgic
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Dissertations / Theses on the topic "Mandible, abnormalities"

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Ratcliffe, Peter H. "The development of surgical procedures for the correction of acquired or developmental anomalies of the mandible." Thesis, The University of Sydney, 1985. http://hdl.handle.net/2123/4756.

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Zhang, Wenbiao, and 張文彪. "Biochemical modulation and stem cell therapy for irradiated mandible." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2009. http://hub.hku.hk/bib/B43224167.

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Xue, Fan, and 薛凡. "Identification of SNP markers on 1p36 and analysis of the association of EPB41 with mandibular prognathism." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2011. http://hub.hku.hk/bib/B45824514.

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McMillan, Brian D. "The intraoral inverted 'L' osteotomy for mandibular advancement." Thesis, 1997. http://hdl.handle.net/2440/122354.

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This study investigates the intraoral inverted 'L' osteotomy for mandibular advancement. The stability of the intraoral inverted 'L' osteotomy is assessed by cephalometric analysis over the short, medium and long term and this is compared to the stability of the bilateral sagittal split osteotomy and the extraoral inverted 'L' osteotomy. The thesis investigates also the incidence of neurosensory disturbance following inverted 'L' osteotomy and comparedit to bilatteral saggittal split osteotomy.<br>Thesis (M.D.S.) -- University of Adelaide, Dept. of Dentistry, 1997.
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Books on the topic "Mandible, abnormalities"

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Krekmanov, Leonard. Orthognathic surgery without the use of postoperative intermaxillary fixation: A clinical and cephalometric evaluation of surgical correction of mandibular and maxillary deformities. Department of Oral Surgery, University of Göteborg, 1989.

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Pirttiniemi, Pertti. Associations of mandibulofacial asymmetries, with special reference to glenoid fossa remodelling. Dept. of Oral Development and Orthodontics, Institute of Dentistry, University of Oulu, 1992.

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Obwegeser, Hugo L. Mandibular growth anomalies: Terminology, aetiology, diagnosis, treatment. Springer, 2001.

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Early Orthodontic Treatment. QUINTESSENCE, 2000.

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Book chapters on the topic "Mandible, abnormalities"

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Garoushi, Ibrahim H., Ramy R. Elbeialy, Amr Gibaly, and Mohammed Atef. "Osteotomy Challenges for Implant Placement in Posterior Mandible." In Osteotomy Essentials - From Basic Techniques to Advanced Practices [Working Title]. IntechOpen, 2024. http://dx.doi.org/10.5772/intechopen.1007618.

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The posterior mandibular region poses significant challenges for dental implantologists due to its unique anatomical constraints. This chapter delves into the complexities of inserting root-form dental implants in this region, focusing on the difficulties and complications that arise from anatomical considerations. A particular emphasis is placed on inferior alveolar nerve lateralization (IANL) surgical technique, which has expanded implant placement possibilities but is also linked with significant risks and drawbacks. The chapter provides an in-depth review of the history and progress of IAN
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Robinson, Max, Keith Hunter, Michael Pemberton, and Philip Sloan. "Salivary gland diseases." In Soames' & Southam's Oral Pathology. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780199697786.003.0009.

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The salivary glands consist of three paired major glands—parotid, sub­mandibular, and sublingual—and the countless minor salivary glands found in almost every part of the oral cavity, except the gingiva and anterior regions of the hard palate. The secretion of saliva is essential for the normal function and health of the mouth, and disorders of salivary gland function predispose to oral disease. Functional disorders in salivary secretion may be associated with primary salivary gland disease but in other cases are a consequence of systemic factors, such as medi­cations, endocrine disturbances,
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Conference papers on the topic "Mandible, abnormalities"

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Hagandora, Catherine K., and Alejandro J. Almarza. "A Comparison of the Mechanical Properties of the Goat Temporomandibular Joint Disc to the Mandibular Condylar Cartilage in Unconfined Compression." In ASME 2011 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2011. http://dx.doi.org/10.1115/sbc2011-53173.

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The temporomandibular joint (TMJ) is a synovial, bilateral joint formed by the articulation of the condyle of the mandible and the articular eminence and glenoid fossa of the temporal bone. The articulating tissues of the joint include the TMJ disc and the mandibular condylar cartilage (MCC). It is estimated that 10 million Americans are affected by TMJ disorders (TMDs), a term encompassing a variety of conditions which result in positional or structural abnormalities in the joint. [1] Characterization of the properties of the articulating tissues of the joint is a necessary prequel to underst
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Mori, Shintaro, Takeshi Hara, Motoki Tagami, et al. "Automated detection of abnormalities in paranasal sinus on dental panoramic radiographs by using contralateral subtraction technique based on mandible contour." In SPIE Medical Imaging, edited by Carol L. Novak and Stephen Aylward. SPIE, 2013. http://dx.doi.org/10.1117/12.2007820.

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