Oral findings in patients with Apert Syndrome

Autor: Gisele da Silva Dalben, Lucimara Teixeira das Neves, Marcia Ribeiro Gomide

Publikováno v: Journal of Applied Oral Science v.14 n.6 2006
Journal of applied oral science
Universidade de São Paulo (USP)
instacron:USP
Journal of Applied Oral Science, Volume: 14, Issue: 6, Pages: 465-469, Published: DEC 2006
Journal of Applied Oral Science

INTRODUCTION: The Apert syndrome is a rare disorder of autosomal dominant inheritance caused by mutations in the FGFR2 gene at locus 10q26; patients with this syndrome present severe syndactyly, exophthalmia, ocular hypertelorism and hypoplastic midf

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http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1678-77572006000600014