1.
Am J Med Genet A
; 149A(3): 519-20, 2009 Mar.
Artículo
en Inglés
| MEDLINE
| ID: mdl-19206156
Asunto(s)
Anomalías Múltiples/patología , Anoftalmos/patología , Nariz/anomalías , Fenotipo , Cráneo/anomalías , Anoftalmos/diagnóstico por imagen , Encéfalo/anomalías , Craneosinostosis/diagnóstico por imagen , Craneosinostosis/patología , Humanos , Lactante , Discapacidad Intelectual/patología , Masculino , Nariz/patología , Índice de Severidad de la Enfermedad , Cráneo/diagnóstico por imagen , Síndrome , Ultrasonografía
2.
Quintessence Int
; 39(3): 251-6, 2008 Mar.
Artículo
en Inglés
| MEDLINE
| ID: mdl-18618041
RESUMEN
Ehlers-Danlos syndrome (EDS) is a hereditary disorder of the connective tissue related to collagen metabolism. Deficiency or alteration of the collagen present in the tissues results in some classic signs such as skin hyperelasticity, articular hypermobility, and vascular fragility, among others. In addition, EDS oral manifestations are rarely cited in the literature. The aim of this article is to report a rare case of a young female patient with EDS who presented supernumerary teeth and an odontogenic keratocyst. There is no report in the literature of the simultaneous occurrence of these alterations. The article further highlights the importance of EDS diagnosis in patients who need dental treatment and the due care for their assistance.