Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
1.
Med Oral Patol Oral Cir Bucal ; 23(2): e168-e179, 2018 Mar 01.
Artículo en Inglés | MEDLINE | ID: mdl-29476678

RESUMEN

BACKGROUND: Oral manifestations are common in neurofibromatosis 1 (NF1), and include jaws and teeth alterations. Our aim was to investigate the craniomaxillofacial morphology of Brazilian children, adolescents and adults with NF1 using cone beam computed tomography. MATERIAL AND METHODS: This study was conducted with 36 Brazilian individuals with NF1 with ages ranging from 4 to 75. The participants were submitted to anamnesis, extra and intraoral exam and cephalometric analysis using cone beam computed tomography. Height of the NF1 individuals was compared to the length of jaws and skull base. The results of the cephalometric measurements of the NF1 group were compared with a control group paired by age, gender and skin color. RESULTS: Individuals with NF1 had lower maxillary length (p<0.0001), lower mandibular length (p<0.0001), lower skull base length (p<0.0001). In children and adolescents, the mandible was more posteriorly positioned (p=0.01), when compared with the control group. There was no association between jaws and skull base length with the height of the individuals with NF1. CONCLUSIONS: Brazilian children, adolescents and adults with NF1 have short mandible, maxilla and skull base. Moreover, children and adolescents present mandibular retrusion.


Asunto(s)
Tomografía Computarizada de Haz Cónico , Maxilares/diagnóstico por imagen , Maxilares/patología , Neurofibromatosis 1/complicaciones , Base del Cráneo/diagnóstico por imagen , Base del Cráneo/patología , Adolescente , Adulto , Anciano , Brasil , Estudios de Casos y Controles , Cefalometría , Niño , Preescolar , Femenino , Humanos , Masculino , Persona de Mediana Edad , Estudios Prospectivos , Adulto Joven
2.
J Clin Pediatr Dent ; 39(2): 168-71, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-25823487

RESUMEN

Neurofibromatosis type 1 (NF1) is a common autosomal genetic disorder with a prevalence of 1 in 3,000 births. NF1 is a complex syndrome characterized by many abnormalities and may affect all organ systems. Oral manifestations of NF1 occur frequently, but reports including NF1 children with facial plexiform neurofibromas and oral alterations are scant. Facial plexiform neurofibroma may cause asymmetry, disfigurement and usually arises from the trigeminal nerve. The aim of this paper is to to report three pediatric NF1 cases with facial plexiform neurofibroma presenting with oral manifestations, which were evaluated clinically and radiographically, and also to briefly review the literature. Patients presented with changes in the oral soft tissues, jaws, and teeth ipsilateral to the tumor.


Asunto(s)
Deformidades Dentofaciales/diagnóstico , Neoplasias Faciales/diagnóstico , Neurofibroma Plexiforme/diagnóstico , Neurofibromatosis 1/diagnóstico , Niño , Femenino , Neoplasias Gingivales/diagnóstico , Sobrecrecimiento Gingival/diagnóstico , Humanos , Macroglosia/diagnóstico , Masculino , Maloclusión/diagnóstico , Mandíbula/anomalías , Cóndilo Mandibular/anomalías , Neoplasias de la Lengua/diagnóstico
SELECCIÓN DE REFERENCIAS
Detalles de la búsqueda