Add to ORKGBackground: The present paper describes the general and oral manifestations in a 32-year-old man previously diagnosed with Apert syndrome. Clinical examination revealed features of acrocephalosyndactyly. The patient was found to have a flattened occiput with frontal prominence, abnormal contour of head (brachycephaly), shallow and downward slanting orbits with bilateral proptosis, hypertelorism, retruded midface, and prognathic mandible.Dental anormalies were present in a patient. Intraoral evaluation revealed normal mouth opening with anterior severe skeletal open bite and Byzantine-arch palate, maxillary alveolar ridges with crowding of maxillary and mandibular teeth, poor hygiene with heavy dental calculus and periodontal pseudopocket, d...
Item does not contain fulltextThis case report describes the combined orthodontic and orthognathic m...
Apert’s syndrome is a craniosynostosis syndrome caused by mutations in the gene coding for the fibro...
BACKGROUND: Apert syndrome is a severe developmental malformation, clinically characterised by cran...
Background: The present paper describes the general and oral manifestations in a 32-year-old man pre...
Defined as a rare type I acrocephalosyndactyly syndrome which is clinically characterized by dysmorp...
The aim of the study is to present the oral findings of a patient with Apert Syndrome who applied to...
To report the oral findings, including dental anomalies, ectopic eruption of the maxillary permanent...
ntroduction: The Apert syndrome is a rare disorder of autosomal dominant inheritance caused by mutat...
Apert syndrome (AS) is indeed a rare congenital disorder that falls under the category of acrocephal...
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...
Apert's syndrome (acrocephalosyndactyly) is a developmental malformation characterized by craniosyno...
Apert syndrome is a rare craniosynostosis syndrome characterized by irregular craniosynostosis, midf...
INTRODUCTION: The Apert syndrome is a rare disorder of autosomal dominant inheritance caused by muta...
Apert Syndrome (AS), or type I acrocephalosyndactyly, is a rare, congenital craniosynostosis conditi...
Item does not contain fulltextThis case report describes the combined orthodontic and orthognathic m...
Apert’s syndrome is a craniosynostosis syndrome caused by mutations in the gene coding for the fibro...
BACKGROUND: Apert syndrome is a severe developmental malformation, clinically characterised by cran...
Background: The present paper describes the general and oral manifestations in a 32-year-old man pre...
Defined as a rare type I acrocephalosyndactyly syndrome which is clinically characterized by dysmorp...
The aim of the study is to present the oral findings of a patient with Apert Syndrome who applied to...
To report the oral findings, including dental anomalies, ectopic eruption of the maxillary permanent...
ntroduction: The Apert syndrome is a rare disorder of autosomal dominant inheritance caused by mutat...
Apert syndrome (AS) is indeed a rare congenital disorder that falls under the category of acrocephal...
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...
Apert's syndrome (acrocephalosyndactyly) is a developmental malformation characterized by craniosyno...
Apert syndrome is a rare craniosynostosis syndrome characterized by irregular craniosynostosis, midf...
INTRODUCTION: The Apert syndrome is a rare disorder of autosomal dominant inheritance caused by muta...
Apert Syndrome (AS), or type I acrocephalosyndactyly, is a rare, congenital craniosynostosis conditi...
Item does not contain fulltextThis case report describes the combined orthodontic and orthognathic m...
Apert’s syndrome is a craniosynostosis syndrome caused by mutations in the gene coding for the fibro...
BACKGROUND: Apert syndrome is a severe developmental malformation, clinically characterised by cran...