Cleido cranial dysplasia: report of a family.
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A family case of Cleidocranial Dysplasia is presented. A mother and two adolescent girls were examined. In all three cases, a radiological series was performed over the entire body. Generalized dysplasia in bones, prolonged retention of primary teeth, and delayed eruption of permanent, as well as supernumerary teeth was diagnosed. The citogenetic study with GTG band showed normal 46, XX. Bilateral audiometry in the mother demonstrated a mild to moderate hypoacustic condition. Radiological findings are presented and the importance of early diagnosis is discussed. (+info)
Bifid mandibular condyle: a case report.
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The bifid mandibular condyle is a rare anomaly. A variety of causes are implicated with its development such as developmental origin and trauma. Because of the lack of epidemiological data, there is little information about the real incidence of this malformation. The purpose of this paper is to report a case of bifid mandibular condyle in a 20-year-old woman who referred to a private radiological clinic for routine dental examination. A panoramic radiography incidentally revealed a discrete modification of the left mandibular condyle. Magnetic resonance imaging (MRI) was taken and confirmed the diagnostic proposed. (+info)
Cleidocranial dysplasia: importance of radiographic images in diagnosis of the condition.
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Cleidocranial dysplasia (CCD) is a rare syndrome usually caused by an autosomal dominant gene, although 40% of cases of CCD appear spontaneously with no apparent genetic cause. This condition is characterized by several cranial malformations and underdevelopment, absence of the clavicles, and multiple supernumerary and impacted permanent teeth. The diagnosis of this condition is usually based on the presence of the main features (supernumerary teeth, partial or total absence of one or both the clavicles, and bony malformations) and on clinical and familial evidence. The bony and dental features of CCD may be visualized on radiographic images of the face and skull. Here, we present a familial case of CCD and discuss the importance of dental radiographs in diagnosis of the condition. (+info)
Cervical column morphology related to head posture, cranial base angle, and condylar malformation.
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The present study describes the cervical column as related to head posture, cranial base, and mandibular condylar hypoplasia. Two groups were included in the study. The 'normal' sample comprised 21 subjects, 15 females aged 23-40 years (mean 29.2 years), and six males aged 25-44 years (mean 32.8 years) with neutral occlusion and normal craniofacial morphology. The condylar hypoplasia group comprised the lateral profile radiographs of 11 patients, eight females, and three males, aged 12-38 years (mean 21.6 years). For each individual, a profile radiograph was taken to perform a visual assessment of the morphology of the cervical column. For the normal group only, the profile radiographs were taken in the standardized head posture to measure the head posture and the cranial base angle. Cervical column: Morphological deviations of the cervical column occurred significantly more often in the subjects with condylar hypoplasia compared with the normal group (P < 0.05 and P < 0.01, respectively). The pattern of morphological deviations was significantly more severe in the subjects with condylar hypoplasia compared with the normal group (P < 0.01). Cervical column related to head posture and cranial base: The cervicohorizontal and cranial base angles were statistically larger in females than in males (P < 0.05 and P < 0.01, respectively). No statistically significant age differences were found. Only in females was the cervical lordosis angle (OPT/CVT, P < 0.01), the inclination of the upper cervical spine (OPT/HOR, P < 0.05), and the cranial base angle (n-s-ba, P < 0.05) significantly positively correlated with fusion of the cervical column. These associations were not due to the effect of age. (+info)
Orthodontic orthognathic surgical treatment of a subject with Williams Beuren syndrome a follow-up from 8 to 25 years of age.
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This article presents a survey of characteristic features of Williams-Beuren syndrome (WBS) as reported in the literature and the interdisciplinary treatment of a subject with WBS with special regard to morphological and functional disorders. Typical features of a patient with WBS and his dental development in a follow-up from 8 to 25 years of age are shown. Early orthodontic treatment approaches, later combined orthodontic-orthognathic surgical procedures, and the status 5 years after surgery are presented. (+info)
PCB126 exposure disrupts zebrafish ventricular and branchial but not early neural crest development.
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Three-dimensional relationship between pharyngeal airway and maxillo-facial morphology.
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In this study, to clarify the influence of the maxillo-mandibular bones and cranium on airway morphology, maxillo-facial morphology in patients with jaw deformation was measured using cephalograms and X-ray CT imaging data. Subjects consisted of 25 adult women in whom cephalograms and X-ray CT were taken to diagnose jaw deformation. The data obtained were classified based on skeletal and facial patterns according to Ricketts analysis, and changes in internal diameter, height and volume of the middle pharyngeal airway were observed. The results showed that the internal diameter of the inferior airway expanded anteriorly when the mandibular bone was in the anterior position, and was slightly constricted and elongated vertically when the mandibular bone was posteriorly rotated. This suggests that airway volume is influenced by the anteroposterior position of the mandibular bone, in that it compensates for decreases in its volume by extending its height inferiorly to cope with posterior deviation of the mandibular bone. (+info)
Aryl hydrocarbon receptor-mediated down-regulation of sox9b causes jaw malformation in zebrafish embryos.
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