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dc.contributor.authorPulgar Encinas, Rosa 
dc.contributor.authorGarcía Espona, Juan Ignacio 
dc.contributor.authorNavajas Rodríguez de Mondelo, Jose Manuel
dc.date.accessioned2025-01-24T10:22:50Z
dc.date.available2025-01-24T10:22:50Z
dc.date.issued2001
dc.identifier.citationPulgar Encinas R, García-Espona I, Navajas Rodriguez de Mondelo JM. Amelogenesis imperfecta: diagnosis and resolution of a case with hypoplasia and hypocalcification of enamel, dental agenesis, and skeletal open bite. Quintessence Int. 2001;32(3):183-9. PMID: 12066657.es_ES
dc.identifier.otherPMID: 12066657
dc.identifier.urihttps://hdl.handle.net/10481/100228
dc.description.abstractA case of amelogenesis imperfecta with hypoplasia, hypocalcification of the enamel, congenital absence of teeth 12 and 22, delayed eruption of tooth 23, edge-to-edge incisal relationship, open bite, and bilateral posterior cross bite at the level of the first and second premolars is presented. Lateral skull teleradiography indicated a Class III skeletal pattern of maxillary origin associated with a dolichofacial pattern with multiple indicators of facial hyperdivergence. The patient presented a major esthetic abnormality of the face and required orthodontic treatment prior to a prosthetic solution with full-coverage metal-ceramic crowns in both the maxilla and the mandible. The diagnosis of cases such as this one and the therapeutic implications from an orthodontic and prosthetic standpoint are reported.es_ES
dc.language.isoenges_ES
dc.publisherQuintessence Internationales_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titleAmelogenesis imperfecta: diagnosis and resolution of a case with hypoplasia and hypocalcification of enamel, dental agenesis, and skeletal open bite.es_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES
dc.type.hasVersionAOes_ES


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