Literature DB >> 10635279

Apert syndrome: a case report with discussion of craniofacial features.

R P Paravatty1, A Ahsan, B T Sebastian, K M Pai, P K Dayal.   

Abstract

Apert syndrome is a rare congenital anomaly characterized by acrocephaly, syndactyly, and abnormalities of other organs. It has characteristic features in the orofacial region, affecting the eyes, palate, middle third of face, and uvula. In this case report, the features of Apert syndrome, particularly in relation to the orofacial region, are discussed.

Entities:  

Mesh：

Year:  1999        PMID： 10635279

Source DB:  PubMed          Journal:  Quintessence Int        ISSN： 0033-6572            Impact factor:   1.677


  4 in total

1.  Apert syndrome: report of a case with emphasis on oral manifestations.

Authors:  B Vadiati Saberi; A Shakoorpour
Journal:  J Dent (Tehran)       Date:  2011-06-30

2.  The spectrum of Apert syndrome: phenotype, particularities in orthodontic treatment, and characteristics of orthognathic surgery.

Authors:  Ariane Hohoff; Ulrich Joos; Ulrich Meyer; Ulrike Ehmer; Thomas Stamm
Journal:  Head Face Med       Date:  2007-02-08       Impact factor: 2.151

Review 3.  Oral and craniofacial clinical signs associated to genetic conditions in human identification part I: a review.

Authors:  Fouad Ayoub; Nicole Aoun; Hassan El Husseini; Houssam Jassar; Fida Sayah; Ziad Salameh
Journal:  J Int Oral Health       Date:  2015-05

4.  Apert's syndrome: Report of a rare case.

Authors:  Parul V Bhatia; Purv S Patel; Yesha V Jani; Naresh C Soni
Journal:  J Oral Maxillofac Pathol       Date:  2013-05
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.