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

被引:14
|
作者
Stavropoulos, Dimitrios [1 ]
Hallberg, Ulrika [2 ]
Mohlin, Bengt [1 ]
Hagberg, Catharina [1 ,3 ]
机构
[1] Univ Gothenburg, Dept Orthodont, Inst Odontol, Sahlgrenska Acad, Gothenburg, Sweden
[2] Nord Sch Publ Hlth, Gothenburg, Sweden
[3] Karolinska Inst, Dept Dent Med, Div Orthodont & Paediat Dent, Huddinge, Sweden
关键词
DISFIGUREMENT; RESILIENCE;
D O I
10.1111/j.1365-263X.2010.01079.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Background. Recent research has been focused on those attributes that appear to buffer a person against the stresses and strains of living with a visible difference. Aim. To provide some insight on how young adults with Crouzon syndrome handle their life. Design. Telephone interviews were carried out with eight Crouzon syndrome individuals (six males, two females, mean age 25.4 years) and data were analysed according to the qualitative method of grounded theory. Results. The informants' main concern was to make the best of their situation, showing that even in adverse conditions, as in Crouzon syndrome, several individuals do find ways to live with their difference and to succeed in various aspects of life, using strategies they construct. Such strategies, as identified from the present investigation, were labelled: committed to an engaging activity, avoiding exposed situations, actively launching oneself, struggling with normalizing facial appearance, and lowering the expectations of finding a love partner. Conclusions. The adaptation of successful coping strategies seemed to be crucial in the quest of attainment of higher self-esteem. The more the participants in the study used the coping strategies they had developed over time, the better they handled their life situation, which led to enhanced well-being.
引用
收藏
页码:35 / 42
页数:8
相关论文
共 50 条
  • [21] Obstructive hydrocephalus and Crouzon syndrome
    Levesque, D.
    Coste, V.
    Gimbert, E.
    Duval, M. -V.
    Pedespan, J. -M.
    Lafourcade, J. -P.
    Korobelnik, J. -F.
    JOURNAL FRANCAIS D OPHTALMOLOGIE, 2019, 42 (04): : E165 - E168
  • [22] Crouzon Syndrome: Report in a Family
    Kumar, Dhanya S.
    Murugesan, Devaki
    Murugan, Kandasamy
    Subramanian, Divya
    Maheshwari, S. Uma
    JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH, 2016, 10 (01) : ZJ2 - ZJ3
  • [23] Hand anomalies in Crouzon syndrome
    Anderson, PJ
    Hall, CM
    Evans, RD
    Jones, BM
    Hayward, RD
    SKELETAL RADIOLOGY, 1997, 26 (02) : 113 - 115
  • [24] Ophthalmic sequelae of Crouzon syndrome
    Gray, TL
    Casey, T
    Selva, D
    Anderson, PJ
    David, DJ
    OPHTHALMOLOGY, 2005, 112 (06) : 1129 - 1134
  • [25] Hand anomalies in Crouzon syndrome
    P. J. Anderson
    Christine M. Hall
    Robert D. Evans
    Barry M. Jones
    Richard D. Hayward
    Skeletal Radiology, 1997, 26 : 113 - 115
  • [26] Crouzon syndrome and Chiari malformation
    Martinot, A
    Hue, V
    Cremer, R
    Dhellemmes, P
    Pellerin, P
    Guieu, JD
    Leclerc, F
    ARCHIVES DE PEDIATRIE, 1996, 3 (12): : 1278 - 1279
  • [27] MULTIDISCIPLINARY MANAGEMENT OF CROUZON SYNDROME
    TURVEY, TA
    LONG, RE
    HALL, DJ
    JOURNAL OF THE AMERICAN DENTAL ASSOCIATION, 1979, 99 (02): : 205 - 209
  • [28] Hearing and otopathology in Crouzon syndrome
    Orvidas, LJ
    Fabry, LB
    Diacova, S
    McDonald, TJ
    LARYNGOSCOPE, 1999, 109 (09): : 1372 - 1375
  • [29] GERMINAL MOSAICISM IN CROUZON SYNDROME
    ROLLNICK, BR
    CLINICAL GENETICS, 1988, 33 (03) : 145 - 150
  • [30] Treatment of Crouzon's syndrome
    Persing, JA
    11TH INTERNATIONAL CONGRESS OF NEUROLOGICAL SURGERY, VOLS 1 AND 2, 1997, : 255 - 259