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Dermatol Clin ; 39(1): 117-127, 2021 Jan.
Article in English | MEDLINE | ID: mdl-33228855

ABSTRACT

The authors collected demographics and assessed the impact of vitiligo using Vitiligo Quality of Life (VitiQoL) and Vitiligo Impact Scale (VIS), followed by a focused survey and semistructured interviews with 22 participants in midwestern Nepal. VitiQoL and VIS scales did not indicate a large impact on quality of life; however, through interviews/focused surveys, participants expressed unhappiness/worry, problems in finding partners, securing employment, and social discrimination due to their skin lesions. These stressors are highlighted along with lack of proper physician counseling and vitiligo-related myths, which create psychosocial distress that may not be given priority in underdeveloped countries like Nepal.


Subject(s)
Psychological Distress , Psychosocial Functioning , Quality of Life , Vitiligo/psychology , Adult , Female , Health Knowledge, Attitudes, Practice , Health Promotion , Humans , Male , Nepal , Qualitative Research , Social Discrimination/psychology , Social Stigma , Surveys and Questionnaires
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