Literature DB >> 23060386

Crouzon syndrome: a social stigma.

Neelisha Pandey1, Ramesh Kumar Pandey, Rajeev Kumar Singh, Naveen Kumar Shah.   

Abstract

Crouzon syndrome is a rare genetic disorder caused due to genetic mutations. It is characterised by partial hearing loss, dry eyes, strabismus and underdevelopment of the upper jaw with facial deformities and malocclusion. These facial deformities greatly affect the social and emotional development of the affected child. The present case report highlights the social problems faced by a child suffering with Crouzon syndrome.

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Year:  2012        PMID: 23060386      PMCID: PMC4544844          DOI: 10.1136/bcr-2012-007242

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  9 in total

Review 1.  Ocular manifestations of Apert and Crouzon syndromes: qualitative and quantitative findings.

Authors:  Sven Kreiborg; M Michael Cohen
Journal:  J Craniofac Surg       Date:  2010-09       Impact factor: 1.046

Review 2.  Preventing behavioural and emotional problems in children who have a developmental disability: a public health approach.

Authors:  Trevor G Mazzucchelli; Matthew R Sanders
Journal:  Res Dev Disabil       Date:  2011-08-09

Review 3.  Management of craniosynostoses.

Authors:  D Renier; E Lajeunie; E Arnaud; D Marchac
Journal:  Childs Nerv Syst       Date:  2000-11       Impact factor: 1.475

4.  Living with Crouzon syndrome: how do young adults with Crouzon syndrome handle their life situation?

Authors:  Dimitrios Stavropoulos; Ulrika Hallberg; Bengt Mohlin; Catharina Hagberg
Journal:  Int J Paediatr Dent       Date:  2011-01       Impact factor: 3.455

5.  Parents' emotion expression as a predictor of child's social competence: children with or without intellectual disability.

Authors:  S Green; B Baker
Journal:  J Intellect Disabil Res       Date:  2011-01-18

6.  Crouzon syndrome.

Authors:  Ernest L Bowling; Fernando D Burstein
Journal:  Optometry       Date:  2006-05

7.  Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome.

Authors:  W Reardon; R M Winter; P Rutland; L J Pulleyn; B M Jones; S Malcolm
Journal:  Nat Genet       Date:  1994-09       Impact factor: 38.330

8.  Fibroblast growth factor receptor 3 (FGFR3) transmembrane mutation in Crouzon syndrome with acanthosis nigricans.

Authors:  G A Meyers; S J Orlow; I R Munro; K A Przylepa; E W Jabs
Journal:  Nat Genet       Date:  1995-12       Impact factor: 38.330

9.  Epigenetics of early child development.

Authors:  Chris Murgatroyd; Dietmar Spengler
Journal:  Front Psychiatry       Date:  2011-04-18       Impact factor: 4.157

  9 in total
  1 in total

1.  Stigma and psychological distress among pediatric participants in the FD/MAS Alliance Patient Registry.

Authors:  Amanda Konradi
Journal:  BMC Pediatr       Date:  2021-04-14       Impact factor: 2.125

  1 in total

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