Literature DB >> 9078640

Dentofacial features of a family with Crouzon syndrome. Case reports.

S L Singer1, I Walpole, W F Brogan, J Goldblatt.   

Abstract

Crouzon syndrome is an autosomal dominant condition characterized by craniosynostosis with associated dentofacial anomalies. This paper describes the variable clinical features in affected individuals over two generations of a family with particular reference to the dentofacial deformities and discussion of management strategies.

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Year:  1997        PMID: 9078640     DOI: 10.1111/j.1834-7819.1997.tb00089.x

Source DB:  PubMed          Journal:  Aust Dent J        ISSN: 0045-0421            Impact factor:   2.291


  2 in total

1.  Familial Crouzon syndrome.

Authors:  Y Samatha; T Harsha Vardhan; A Ravi Kiran; A J Sai Sankar; B Ramakrishna
Journal:  Contemp Clin Dent       Date:  2010-10

2.  Crouzon syndrome: clinico-radiological illustration of a case.

Authors:  Raviprakash Sasankoti Mohan; Naveen Shanker Vemanna; Sankalp Verma; Neha Agarwal
Journal:  J Clin Imaging Sci       Date:  2012-11-30
  2 in total

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