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Int J Oral Maxillofac Surg ; 39(6): 622-5, 2010 Jun.
Article in English | MEDLINE | ID: mdl-20144538

ABSTRACT

A 12-year-old girl with an otherwise typical Marfan syndrome (Ghent criteria fulfilled) presented with highly unusual oral manifestations consisting of supernumerary teeth and severe dental crowding. Pathological examination of the supernumerary teeth revealed an elevated number of pulpoliths. No mutation in the FBN1, TGFBR1 and TGFBR2 genes was identified despite exhaustive screening, suggesting that another gene defect could explain this association of marfanoid features with dental abnormalities.


Subject(s)
Dental Pulp Diseases/etiology , Marfan Syndrome/complications , Tooth, Supernumerary/etiology , Child , Dental Pulp Diseases/genetics , Female , Fibrillin-1 , Fibrillins , Humans , Malocclusion/etiology , Microfilament Proteins/genetics , Protein Serine-Threonine Kinases/genetics , Receptor, Transforming Growth Factor-beta Type I , Receptor, Transforming Growth Factor-beta Type II , Receptors, Transforming Growth Factor beta/genetics , Tooth, Supernumerary/genetics
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