Literature DB >> 23120355

Crouzon syndrome: A case report and review of literature.

Harroop Kaur1, Harmeet Singh Waraich, Chander Mohan Sharma.   

Abstract

Crouzon syndrome, also called craniofacial dysostosis is an autosomal dominant disorder characterized by premature closure of cranial sutures, midfacial hypoplasia and orbital defects. Herein we report a case of this rare entity who presented with brachycephaly, maxillary hypoplasia, wide parrot beaked nose, repaired bilateral cleft lip and cleft palate along with dental and orbital abnormalities.

Entities:  

Keywords:  Crouzon syndrome; craniosynostosis; maxillary hypoplasia

Year:  2006        PMID： 23120355      PMCID： PMC3450369          DOI： 10.1007/BF03049602

Source DB:  PubMed          Journal:  Indian J Otolaryngol Head Neck Surg        ISSN： 2231-3796


  5 in total

Review 1.  Fibroblast growth factor receptor-2 mutations in craniosynostosis.

Authors:  S Malcolm; W Reardon
Journal:  Ann N Y Acad Sci       Date:  1996-06-08       Impact factor: 5.691

2.  Crouzon syndrome: cephalometric analysis and evaluation of pathogenesis.

Authors:  F Carinci; A Avantaggiato; C Curioni
Journal:  Cleft Palate Craniofac J       Date:  1994-05

3.  Hydrocephalus and mental retardation in craniosynostosis.

Authors:  M J Noetzel; J L Marsh; H Palkes; M Gado
Journal:  J Pediatr       Date:  1985-12       Impact factor: 4.406

4.  Craniosynostosis: surgical treatment during the first year of life.

Authors:  C di Rocco; E Marchese; F Velardi
Journal:  J Neurosurg Sci       Date:  1992 Jul-Sep       Impact factor: 2.279

5.  Clinical findings precede objective diagnostic testing in the identification of increased ICP in syndromic craniosynostosis.

Authors:  Lisa R David; Emily Velotta; R Grey Weaver; John A Wilson; Louis C Argenta
Journal:  J Craniofac Surg       Date:  2002-09       Impact factor: 1.046
  5 in total
  7 in total

1.  Premature craniosynostosis in a rare genetic disease- a case report.

Authors:  Hasnain Abbas Dharamshi; Tufail Raza; Ali Abbas Mohsin Ali; Zuhair Lilani; Syed Zohaib Ahsan; Ahmad Faraz; Syeda Tahira Naqvi
Journal:  Iran J Public Health       Date:  2015-03       Impact factor: 1.429

2.  Clinical characteristics of Crouzon syndrome.

Authors:  L Balyen; L S Deniz Balyen; S Pasa
Journal:  Oman J Ophthalmol       Date:  2017 May-Aug

3.  Computed tomography findings of Crouzon syndrome: A case report.

Authors:  Juan Guillermo Arámbula Neira; Valeria Del Castillo Herazo; Nury Tatiana Rincón Cuenca; Angélica M Sanabria Cano; Maryi Fernanda Bermudez Sarmiento; María F Castro; Andrés Felipe Herrera Ortiz
Journal:  Radiol Case Rep       Date:  2022-02-17

4.  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

5.  Crouzon's Syndrome: A Case Report.

Authors:  G Ravi Kumar; M Jyothsna; Syed Basheer Ahmed; K Sree Lakshmi
Journal:  Int J Clin Pediatr Dent       Date:  2013-04-26

6.  FGFR2 mutations and associated clinical observations in two Chinese patients with Crouzon syndrome.

Authors:  Ying Lin; Hongbin Gao; Siming Ai; Jacob V P Eswarakumar; Yi Zhu; Chuan Chen; Tao Li; Bingqian Liu; Hongye Jiang; Yuhua Liu; Yonghao Li; Qingxiu Wu; Haichun Li; Xiaoling Liang; Chenjin Jin; Xinhua Huang; Lin Lu
Journal:  Mol Med Rep       Date:  2017-08-29       Impact factor: 2.952

7.  Imaging diagnosis of Crouzon syndrome in two cases confirmed on genetic studies - with a brief review.

Authors:  Shabnam Bhandari Grover; Aanchal Bhayana; Hemal Grover; Seema Kapoor; Harish Chellani
Journal:  Indian J Radiol Imaging       Date:  2019-12-31
  7 in total

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