Craniofacial Anomalies
Mostrando 13-24 de 84 artigos, teses e dissertações.
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13. Rehabilitative treatment of cleft lip and palate: experience of the Hospital for Rehabilitation of Craniofacial Anomalies/USP (HRAC/USP) Part 4: Oral Rehabilitation
Treatment of patients with cleft lip and palate is completed with fixed prostheses, removable, total, implants and aims to restore aesthetics, phonetics and function and should be guided by the basic principles of oral rehabilitation, such as physiology, stability, aesthetics, hygiene and the expectations of the patient. In order to obtain longevity of a pro
J. Appl. Oral Sci.. Publicado em: 2013-06
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14. The relationship between the speech perception and the degree of satisfaction among adult users of cochlear implants
INTRODUCTION: In recent years, the benefits associated with the use of cochlear implants (CIs), especially with regard to speech perception, have proven to surpass those produced by the use of hearing aids, making CIs a highly efficient resource for patients with severe/profound hearing loss. However, few studies so far have assessed the satisfaction of adul
Int. Arch. Otorhinolaryngol.. Publicado em: 2013-06
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15. Rehabilitative treatment of cleft lip and palate: experience of the Hospital for Rehabilitation of Craniofacial Anomalies - USP (HRAC-USP) - part 3: Oral and Maxillofacial Surgery
This paper presents the treatment protocol of maxillofacial surgery in the rehabilitation process of cleft lip and palate patients adopted at HRAC-USP. Maxillofacial surgeons are responsible for the accomplishment of two main procedures, alveolar bone graft surgery and orthognathic surgery. The primary objective of alveolar bone graft is to provide bone tiss
J. Appl. Oral Sci.. Publicado em: 2012-12
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16. Rehabilitative treatment of cleft lip and palate: experience of the Hospital for Rehabilitation of Craniofacial Anomalies - USP (HRAC-USP) - Part 2: Pediatric Dentistry and Orthodontics
The aim of this article is to present the pediatric dentistry and orthodontic treatment protocol of rehabilitation of cleft lip and palate patients performed at the Hospital for Rehabilitation of Craniofacial Anomalies - University of São Paulo (HRAC-USP). Pediatric dentistry provides oral health information and should be able to follow the child with cleft
J. Appl. Oral Sci.. Publicado em: 2012-04
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17. Rehabilitative treatment of cleft lip and palate: experience of the Hospital for Rehabilitation of Craniofacial Anomalies/USP (HRAC/USP) - Part 1: overall aspects
Cleft lip and palate is the most common among craniofacial malformations and causes several esthetic and functional implications that require rehabilitation. This paper aims to generally describe the several aspects related to this complex pathology and the treatment protocol used by the Hospital for Rehabilitation of Craniofacial Anomalies, University of S�
Journal of Applied Oral Science. Publicado em: 2012-02
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18. Distance Learning Course in Scientific Writing in English on Craniofacial Anomalies. / Curso a distância de redação científica na Língua Inglesa na área de anomalias craniofaciais
Introdução: A importância da Língua Inglesa para a ciência é indiscutível e a comunidade científica deve ter o aprendizado desta como base para sua internacionalização. Objetivos: O objetivo deste estudo foi elaborar e avaliar um curso a distância de suporte de escrita científica para a redação de abstracts na Língua Inglesa, na área de Anoma
IBICT - Instituto Brasileiro de Informação em Ciência e Tecnologia. Publicado em: 16/12/2011
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19. Goldenhar syndrome: clinical features with orofacial emphasis
OBJECTIVES: Goldenhar syndrome (GS) is a relatively common developmental disorder characterized by craniofacial anomalies in association with vertebral, cardiac, renal, and central nervous system defects. This paper describes GS features with special emphasis on oral characteristics. MATERIAL AND METHODS: The clinical features of 6 patients with GS aged 3 mo
Journal of Applied Oral Science. Publicado em: 2010-12
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20. Timing and sequence of primary tooth eruption in children with cleft lip and palate
OBJECTIVE: To determine the timing and sequence of eruption of primary teeth in children with complete bilateral cleft lip and palate. MATERIAL AND METHODS: This cross-sectional study was conducted at the Hospital for Rehabilitation of Craniofacial Anomalies of the University of São Paulo, Bauru, SP, Brazil, with a sample of 395 children (128 girls and 267
Journal of Applied Oral Science. Publicado em: 2010-06
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21. Rotavirus gastroenteritis in a children's hospital specialized in craniofacial malformations
This study aimed to verify the relationship between acute diarrhea provoked by rotavirus and different indicators of craniofacial malformations. In the Hospital for Rehabilitation of Craniofacial Anomalies, 8,724 children with cleft lip and cleft palate were divided into the following groups: acute diarrhea and infection due to rotavirus (C1, n = 62), acute
Journal of Venomous Animals and Toxins including Tropical Diseases. Publicado em: 2010
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22. Neurodevelopmental risk factors in schizophrenia
The authors review environmental and neurodevelopmental risk factors for schizophrenic disorders, with emphasis on minor physical anomalies, particularly craniofacial anomalies and dermatoglyphic variations. The high prevalence of these anomalies among schizophrenic subjects supports the neurodevelopmental theory of the etiology of schizophrenia, since they
Publicado em: 2010
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23. Refinamento citogenético em indivíduos com anomalias craniofaciais sindômicas sem diagnóstico definido / Cytogenetic refinement in individuals with syndromic craniofacial anomalies with unkown diagnoses
Objetivos: Investigar possíveis alterações citogenéticas, através da técnica de bandamento de alta resolução, em indivíduos com anomalias craniofaciais associadas ao atraso no desenvolvimento neuropsicomotor e sem diagnóstico clínico-genético definido, com cariótipo (com bandas) prévio normal e estabelecer possível correlação entre o fenóti
Publicado em: 2010
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24. Manifestações bucais em pacientes com síndrome de Kabuki
Kabuki syndrome (KS, Kabuki make-up syndrome, Niikawa-Kuroki syndrome) is a rare genetic disorder characterized by multiple congenital anomalies and mental retardation. The diagnosis is clinical and based on the findings described simultaneously in independent studies of two groups in Japan. The sample comprised sixteen KS individuals diagnosed by Department
Publicado em: 2010