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1.
Eur J Paediatr Dent ; 17(1): 29-33, 2016 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-26949236

RESUMEN

AIM: To develop a theoretical aepidemiological model for the prediction of orthodontic workforce needs, based on regional orthodontic treatment need. MATERIALS AND METHODS: Data were collected for the number of children between the ages of 8-11 years attending primary schools in Greece, within each regional division. Treatment need of the children was estimated using the Index of Orthodontic Treatment Need (IOTN). Demographics of practicing orthodontists in Greece were also collected. Based on the distribution of orthodontists and the number of children per region who would potentially receive orthodontic treatment (IOTN 3-5), the presence and distribution of orthodontic manpower was evaluated. RESULTS: Overall orthodontic manpower is sufficient for Greece's needs with an excess of 55 orthodontists. Distribution however is not uniform, and this ranges from a large underrepresentation of orthodontists in the Ionian Islands (47% of those required) to an overrepresentation in the Attica region (183% of those required). CONCLUSION: Based on the present theoretical model, Greece has an adequate overall orthodontic workforce for coverage of the population needs, but with large regional variations indicating that some regions have a surplus while others a shortage of orthodontists. The present model seems suitable for the calculation of regional orthodontic workforce coverage of a population.


Asunto(s)
Evaluación de Necesidades/estadística & datos numéricos , Ortodoncistas/estadística & datos numéricos , Niño , Predicción , Grecia/epidemiología , Humanos , Indice de Necesidad de Tratamiento Ortodóncico/estadística & datos numéricos , Maloclusión/epidemiología , Modelos Teóricos , Ortodoncistas/provisión & distribución
2.
Angle Orthod ; 82(3): 556-64, 2012 May.
Artículo en Inglés | MEDLINE | ID: mdl-22050072

RESUMEN

The auriculo-condylar syndrome is caused by abnormalities of the first and second pharyngeal arches during embryonic development. Its inheritance follows the autosomal dominant pattern. Both familial and individual cases are reported in the literature. The syndrome is characterized by wide phenotypic variation, with affected individuals expressing clinical signs of variable severity due to variable expressivity of the responsible genes. Clinical signs of the syndrome include auricular malformation, hypoplasia of the mandibular condyles, anomalies of the temporomandibular joints, malocclusion, and, in more severe cases, cleft palate, glossoptosis, facial asymmetry, and respiratory problems. The aim of this article is to report a case of a female patient with signs of the auriculo-condylar syndrome and to present the pedigree of her family. Clinical findings, diagnosis, treatment plan, and final treatment are analyzed.


Asunto(s)
Enfermedades del Oído/patología , Oído/anomalías , Mandíbula/anomalías , Cóndilo Mandibular/anomalías , Retrognatismo/patología , Cefalometría , Niño , Oído/patología , Oído/cirugía , Enfermedades del Oído/cirugía , Asimetría Facial/patología , Femenino , Humanos , Maloclusión de Angle Clase III/terapia , Mandíbula/cirugía , Ortodoncia Correctiva , Procedimientos Quirúrgicos Ortognáticos , Osteogénesis por Distracción , Linaje
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