Facial Bones
Mostrando 25-36 de 48 artigos, teses e dissertações.
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25. ORAL AND MAXILLOFACIAL TRAUMA IN ASSAULT: A STUDY IN A HOSPITAL ON THE OUTSKIRTS OF SÃO PAULO / "Traumatismos buco maxilo faciais por agressão: estudo em hospital da periferia do município de São Paulo"
SUMMARY ORAL AND MAXILLOFACIAL TRAUMA IN ASSAULT: A STUDY IN A HOSPITAL ON THE OUTSKIRTS OF SÃO PAULO There has been an expressive increase in all forms of violence in todays society, specially the physical violence, which most of the times affects the face. This study aimed to review the charts of 493 patients victims of assault seen between december 200
Publicado em: 2002
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26. The midline craniofacial skeleton in holoprosencephalic fetuses.
Craniofacial skeletal development in eight human holoprosencephalic fetuses from second trimester abortions were examined by radiography and histology. The whole spectrum of associated facial malformations from anophthalmia through cyclopia, ethmocephaly, cebocephaly, and median cleft lip to short philtrum was represented. Cases with the most severe facial m
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27. Clinical Pathology of Fibro-Osteo-Cemental Lesions in the Cranio-Facial Jaw Bones. (A new approach to differential diagnosis.)
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28. Temporohyoid osteoarthropathy and unilateral facial nerve paralysis in a horse
A 13-year-old broodmare was referred for weight loss and left facial nerve paralysis. Bilateral temporohyoid osteoarthropathy was diagnosed based on proliferation of the temporohyoid joints and stylohyoid bones on radiographs and guttural pouch endoscopy. The left side was more severely affected. Treatment resulted in little or no improvement.
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29. Migration of craniofacial periosteum in growing guinea-pigs.
The use of a carbon particle tattoo provided stable periosteal markers and a means of recording periosteal movement both anteroposteriorly and transversely during growth in guinea-pigs. In general, the periosteum migrated toward the cranial sutures. The radial pattern, demonstrated on the frontal bones and indicated on the nasal and parietal bones, showed th
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30. Sclerosteosis in a Spanish male: first report in a person of Mediterranean origin.
We report the first observation of sclerosteosis in Spain. To the best of our knowledge, this is the first case of sclerosteosis in a person of Mediterranean origin with no known Dutch ancestors. He has the characteristic phenotype of the disease with right facial nerve palsy and syndactyly and the typical radiological features, including generalised bone sc
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31. Microtia and short stature: a new syndrome.
Bilateral microtia, absent patellae, short stature, poor weight gain, and characteristic facial features are described in two female sibs. Other skeletal anomalies included complete habitual dislocation of the elbow, slender ribs and long bones, abnormal modelling of the glenoid fossae with hooked clavicles, and clinodactyly. Bone age was significantly delay
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32. Evolution and development of facial bone morphology in threespine sticklebacks
How do developmental mechanisms evolve to control changing skeletal morphology, the shapes and sizes of individual bones? We address this question with studies of the opercle (OP), a large facial bone that has undergone marked morphological evolution in the ray-finned fish. Attributes for developmental analysis motivated us to examine how OP shape and size e
National Academy of Sciences.
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33. Further delineation of the Yunis-Varon syndrome.
A boy with intrauterine growth retardation, microcephaly, dysostosis of the skull, hypoplastic facial bones, labiogingival retraction, agenesis of the clavicles, distal aphalangia, and severely hypoplastic thumbs and halluces is described. The features are consistent with the Yunis-Varon syndrome. Review of published reports shows this to be a generalised di
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34. Spondyloenchondrodysplasia.
Spondyloenchondrodysplasia is a rare autosomal recessive skeletal dysplasia with vertebral dysplasia and enchondroma-like lesions in the pelvis and long bones. The vertebral bodies show dorsally accentuated platyspondyly with disturbance of ossification. Clinical abnormalities such as short stature, rhizomelic micromelia, increased lumbar lordosis, barrel ch
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35. The surgical treatment of fibrous dysplasia. With emphasis on recent contributions from cranio-maxillo-facial surgery.
Fibrous dysplasia is a congenital, metabolic, nonfamilial disturbance that occurs in one or more bones, at times in association with skin pigmentations or endocrine abnormalities. The authors report on a large personal series of 23 patients with fibrous dysplasia involving the craniofacial skeleton. The etiology, clinical findings, pathology, and differentia
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36. The Baller-Gerold syndrome.
A case of severe craniosynostosis-radial aplasia (Baller-Gerold) syndrome is described in a newborn male, following a pregnancy complicated by polyhydramnios and intrauterine growth retardation. Death occurred after two hours owing to a prolonged apnoeic spell. Extensive agenesis of the frontal and parietal bones, resulting in a very large fontanelle, in add