Literature DB >> 27001554

The Role of Appearance in Adolescents' Experiences of Neurofibromatosis Type 1: A Survey of Young People and Parents.

Jenny Barke1, Jane Coad2, Diana Harcourt3.   

Abstract

Neurofibromatosis type 1 (NF1) is a genetic condition which can result in varying degrees of visible difference (disfigurement). Adolescence is a time when appearance concerns become more salient for many young people and is acknowledged as a particularly challenging time for individuals with NF1. There is currently little research into the psychosocial impact of the appearance changes associated with NF1 during this stage of life. In order to address this, surveys of young people with NF1 aged 14-24 years (n = 73), and parents of young people with NF1 (n = 55) were developed following interview studies with these groups. The surveys included the Perceived Stigma Questionnaire, Social Comfort Questionnaire, Body Esteem Scale (appearance subscale) and the Subjective Happiness Scale. Young people and parents identified appearance as central to young peoples' experience of NF1, however no significant difference was found on measures of body esteem, happiness, stigma or social comfort between those young people who reported their NF1 was noticeable to others and those who reported it was not. Findings from the parent survey indicated that their reports of greater perceived noticeability did relate to greater perceived stigma and lower levels of social comfort. Findings highlight the importance of attending to young people's concerns around appearance in general and managing the possibility of future appearance changes, rather than the current noticeability of NF1.

Entities:  

Keywords:  Appearance; Body image; NF1; Neurofibromatosis Type 1; Parents; Psychosocial; Young people

Mesh:

Year:  2016        PMID: 27001554     DOI: 10.1007/s10897-016-9944-y

Source DB:  PubMed          Journal:  J Genet Couns        ISSN: 1059-7700            Impact factor:   2.537


  29 in total

1.  The romantic experiences of adolescents with a visible difference: exploring concerns, protective factors and support needs.

Authors:  Catrin Griffiths; Heidi Williamson; Nichola Rumsey
Journal:  J Health Psychol       Date:  2012-01-17

2.  The reliability and validity of the Perceived Stigmatization Questionnaire (PSQ) and the Social Comfort Questionnaire (SCQ) among an adult burn survivor sample.

Authors:  John W Lawrence; James A Fauerbach; Leslie J Heinberg; Marion Doctor; Brett D Thombs
Journal:  Psychol Assess       Date:  2006-03

3.  School-based peer support groups: a new approach to the prevention of disordered eating.

Authors:  Gail L McVey; Melissa Lieberman; Nancy Voorberg; Diana Wardrope; Elizabeth Blackmore
Journal:  Eat Disord       Date:  2003       Impact factor: 3.222

4.  Uncertainty and its relation to the psychological and social correlates of chronic illness in children.

Authors:  D J Jessop; R E Stein
Journal:  Soc Sci Med       Date:  1985       Impact factor: 4.634

5.  Perceived stigmatization and social comfort: validating the constructs and their measurement among pediatric burn survivors.

Authors:  John W Lawrence; Laura Rosenberg; Ruth B Rimmer; Brett D Thombs; James A Fauerbach
Journal:  Rehabil Psychol       Date:  2010-11

Review 6.  Guidelines for the diagnosis and management of individuals with neurofibromatosis 1.

Authors:  Rosalie E Ferner; Susan M Huson; Nick Thomas; Celia Moss; Harry Willshaw; D Gareth Evans; Meena Upadhyaya; Richard Towers; Michael Gleeson; Christine Steiger; Amanda Kirby
Journal:  J Med Genet       Date:  2006-11-14       Impact factor: 6.318

7.  Parents' experiences of caring for a young person with neurofibromatosis type 1 (NF1): a qualitative study.

Authors:  Jenny Barke; Jane Coad; Diana Harcourt
Journal:  J Community Genet       Date:  2015-07-23

8.  Social skills of children with neurofibromatosis type 1.

Authors:  Belinda Barton; Kathryn North
Journal:  Dev Med Child Neurol       Date:  2004-08       Impact factor: 5.449

9.  Visible difference amongst children and adolescents: issues and interventions.

Authors:  Nichola Rumsey; Diana Harcourt
Journal:  Dev Neurorehabil       Date:  2007 Apr-Jun       Impact factor: 2.308

10.  Impact of neurofibromatosis 1 upon quality of life in childhood: a cross-sectional study of 79 cases.

Authors:  P Wolkenstein; D Rodriguez; S Ferkal; H Gravier; V Buret; N Algans; M-C Simeoni; S Bastuji-Garin
Journal:  Br J Dermatol       Date:  2008-12-05       Impact factor: 9.302

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  3 in total

1.  An Internet support group for parents of children with neurofibromatosis type 1: a qualitative analysis.

Authors:  Staci Martin; Kari L Struemph; Alyssa Poblete; Mary Anne Toledo-Tamula; Robin Lockridge; Marie Claire Roderick; Pamela Wolters
Journal:  J Community Genet       Date:  2018-03-02

2.  Lifespan Development: Symptoms Experienced by Individuals with Neurofibromatosis Type 1 Associated Plexiform Neurofibromas from Childhood into Adulthood.

Authors:  Sally E Jensen; Zabin S Patel; Robert Listernick; Joel Charrow; Jin-Shei Lai
Journal:  J Clin Psychol Med Settings       Date:  2019-09

Review 3.  Measuring Happiness in Adolescent Samples: A Systematic Review.

Authors:  Justė Lukoševičiūtė; Gita Argustaitė-Zailskienė; Kastytis Šmigelskas
Journal:  Children (Basel)       Date:  2022-02-08
  3 in total

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