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dc.rights.licenseopenen_US
hal.structure.identifierLaboratoire de psychologie [LabPsy]
dc.contributor.authorFOURNIER, Hugo
hal.structure.identifierLaboratoire de psychologie [LabPsy]
dc.contributor.authorHASDENTEUFEL, Marie
hal.structure.identifierLaboratoire de psychologie [LabPsy]
dc.contributor.authorGARROUTEIGT, Constance
hal.structure.identifierInria Bordeaux - Sud-Ouest
dc.contributor.authorPERIE, Mathieu
dc.contributor.authorGLIKSOHN, Antoine
dc.contributor.authorJOUANNE, Beatrice
hal.structure.identifierLaboratoire de Microbiologie Clinique [AP-HP Hôpital Necker-Enfants Malades]
dc.contributor.authorHADJ-RABIA, Smail
hal.structure.identifierCHU Bordeaux
hal.structure.identifierLaboratoire Maladies Rares: Génétique et Métabolisme (Bordeaux) [U1211 INSERM/MRGM]
dc.contributor.authorARVEILER, Benoit
hal.structure.identifierCHU Bordeaux
dc.contributor.authorMORICE-PICARD, Fanny
hal.structure.identifierLaboratoire de psychologie [LabPsy]
dc.contributor.authorQUINTARD, Bruno
ORCID: 0000-0002-2206-6137
IDREF: 057867968
dc.date.accessioned2024-03-12T17:16:47Z
dc.date.available2024-03-12T17:16:47Z
dc.date.issued2024-01-29
dc.identifier.issn1741-7015en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/188731
dc.description.abstractEnTo date, almost no research on the psychosocial implications of albinism has been conducted in France and an exploration of albinism-related experiences could be beneficial, in order to better understand this condition. The aim of this study was to examine how French people with albinism and their parents live with and adapt to this condition in all the areas of their lives. Semi-structured phone interviews were conducted with 9 parent-child dyads, each participating separately. Participants were recruited by convenience sampling, thanks to the combined efforts of a patient association (Genespoir) and professionals from the partner medical referral centers involved in the project. Dyads in which the individual with albinism had any comorbidity were excluded. The interviews were then transcribed and subjected to in-depth thematic analysis. Two codebooks were constructed in a mirrored process: one for people with albinism; the other for their parents. They were finally merged at the end of the coding step. Four main categories were identified: personal perceptions and social representations of albinism, difficulties and obstacles encountered by people with albinism, resources and facilitators, and the importance of parent-child functioning. The results indicated that experiences of stigmatization during childhood and adolescence are common and that people with albinism face challenges in adapting to certain obstacles related to their visual impairments (VI) (e.g., inability to drive a car; eye strain...). Parents emerged as one, if not as the main, source of support for people with albinism throughout their development. Although external support systems exist to assist them in various aspects of their lives, some of them primarily rely on their own personal resources to cope. This research highlights the importance of a systemic and transdisciplinary approach to make sure families receive the support that best meets their needs.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subject.enAlbinism
dc.subject.enRare diseases
dc.subject.enDyadic functioning
dc.subject.enDisability adjustment
dc.subject.enVisual impairment
dc.subject.enDaily life
dc.subject.enSystemic approach
dc.subject.enQualitative research
dc.title.enThe experience of albinism in France: a qualitative study on dyads of parents and their adult child with albinism.
dc.title.alternativeBMC Meden_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1186/s12916-024-03251-zen_US
dc.subject.halSciences de l'Homme et Société/Psychologieen_US
dc.identifier.pubmed38281904en_US
bordeaux.journalBMC Medicineen_US
bordeaux.page40en_US
bordeaux.volume22en_US
bordeaux.hal.laboratoriesLaboratoire de psychologie (LabPsy) - UR 4139en_US
bordeaux.issue1en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.identifier.funderIDFondation Maladies Raresen_US
bordeaux.import.sourcepubmed
hal.identifierhal-04501801
hal.version1
hal.date.transferred2024-03-12T17:16:51Z
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exporttrue
workflow.import.sourcepubmed
dc.rights.ccCC BYen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=BMC%20Medicine&rft.date=2024-01-29&rft.volume=22&rft.issue=1&rft.spage=40&rft.epage=40&rft.eissn=1741-7015&rft.issn=1741-7015&rft.au=FOURNIER,%20Hugo&HASDENTEUFEL,%20Marie&GARROUTEIGT,%20Constance&PERIE,%20Mathieu&GLIKSOHN,%20Antoine&rft.genre=article


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