SAT0260 PENTOXYFILLINE GEL FOR ORAL ULCERS IN PATIENTS WITH BEHÇET’S SYNDROME

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Oral Findings in Patients with Apert Syndrome

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 midface with Class III malocclusion, besides systemic alterations. Most investigations available on the Apert syndrome address the genetic aspect or sur...

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ژورنال

عنوان ژورنال: Annals of the Rheumatic Diseases

سال: 2020

ISSN: 0003-4967,1468-2060

DOI: 10.1136/annrheumdis-2020-eular.5610