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Cleft Palate Craniofac J ; 57(6): 782-790, 2020 06.
Artigo em Inglês | MEDLINE | ID: mdl-31876171

RESUMO

Klippel-Trenaunay syndrome (KTS) is a congenital disorder associated with capillary, venous, lymphatic vascular malformations, and unilateral hypertrophy of the soft tissue and bone. We report a case of a 5-year-old girl with KTS who was followed up until age 17. The asymmetry of her maxillary dentition became remarkable with growth, although no significant left-right difference in either the maxilla or mandible was recognized. Acceptable occlusion was achieved without fixed orthodontic appliances; however, it was necessary to develop treatment plans in accordance with the general symptoms of the disease.


Assuntos
Síndrome de Klippel-Trenaunay-Weber , Pré-Escolar , Feminino , Humanos , Síndrome de Klippel-Trenaunay-Weber/diagnóstico por imagem , Síndrome de Klippel-Trenaunay-Weber/terapia , Mandíbula/diagnóstico por imagem , Pacientes
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