Add to ORKGApert’s syndrome is a craniosynostosis syndrome caused by mutations in the gene coding for the fibroblast growthfactor receptor 2 (FGFR2), characterized by craniosynostosis, midface hypoplasia and syndactyly of the hands and feet. It has several oral manifestations, such as ogival palate, maxillary transverse and sagittal hypoplasia, dental crowding, eruptive delay and ectopic position of the teeth. The diagnosis of Apert’s syndrome is established in a proband with classic clinical characteristics, and genetic tests can also be performed. Patients with this syndrome often require craniofacial team care and dental, orthodontic and orthognathic surgical management because of their esthetic and functional problems such as Class III maloc...
Introduction: Apert syndrome is a rare type of syndromic craniosynostosis. Patients have an explicit...
INTRODUCTION: The Apert syndrome is a rare disorder of autosomal dominant inheritance caused by muta...
Aim and objective: To present an Apert syndrome patient with midfacial growth deficiency treated wit...
Apert’s syndrome is a craniosynostosis syndrome caused by mutations in the gene coding for the fibro...
Apert Syndrome (AS), or type I acrocephalosyndactyly, is a rare, congenital craniosynostosis conditi...
Treatment the Apert Syndrome is unique, therefore, divergences exist in the priority of the procedur...
Apert syndrome (AS) is indeed a rare congenital disorder that falls under the category of acrocephal...
Background: The present paper describes the general and oral manifestations in a 32-year-old man pre...
The aim of the study is to present the oral findings of a patient with Apert Syndrome who applied to...
Defined as a rare type I acrocephalosyndactyly syndrome which is clinically characterized by dysmorp...
Apert syndrome is named for the French physician. Eugene Apert in 1906 described the syndrome acroce...
A síndrome de Apert é uma craniosinostose causada por mutações no gene codificante do recetor de fat...
Abstract: In this article, an interesting case of Apert syndrome in a 14-year-old boy with character...
Abstract: In this article, an interesting case of Apert syndrome in a 14-year-old boy with character...
BACKGROUND: Apert syndrome is a severe developmental malformation, clinically characterised by cran...
Introduction: Apert syndrome is a rare type of syndromic craniosynostosis. Patients have an explicit...
INTRODUCTION: The Apert syndrome is a rare disorder of autosomal dominant inheritance caused by muta...
Aim and objective: To present an Apert syndrome patient with midfacial growth deficiency treated wit...
Apert’s syndrome is a craniosynostosis syndrome caused by mutations in the gene coding for the fibro...
Apert Syndrome (AS), or type I acrocephalosyndactyly, is a rare, congenital craniosynostosis conditi...
Treatment the Apert Syndrome is unique, therefore, divergences exist in the priority of the procedur...
Apert syndrome (AS) is indeed a rare congenital disorder that falls under the category of acrocephal...
Background: The present paper describes the general and oral manifestations in a 32-year-old man pre...
The aim of the study is to present the oral findings of a patient with Apert Syndrome who applied to...
Defined as a rare type I acrocephalosyndactyly syndrome which is clinically characterized by dysmorp...
Apert syndrome is named for the French physician. Eugene Apert in 1906 described the syndrome acroce...
A síndrome de Apert é uma craniosinostose causada por mutações no gene codificante do recetor de fat...
Abstract: In this article, an interesting case of Apert syndrome in a 14-year-old boy with character...
Abstract: In this article, an interesting case of Apert syndrome in a 14-year-old boy with character...
BACKGROUND: Apert syndrome is a severe developmental malformation, clinically characterised by cran...
Introduction: Apert syndrome is a rare type of syndromic craniosynostosis. Patients have an explicit...
INTRODUCTION: The Apert syndrome is a rare disorder of autosomal dominant inheritance caused by muta...
Aim and objective: To present an Apert syndrome patient with midfacial growth deficiency treated wit...