Ano de Publicação: 2024

 

AUTORIA

Ana Paula Lima de Queiroz1,a, Rodrigo Abensur Athanazio2,b, Mary Anne Kowal Olm3,c, Bruna Rubbo4,5,d, Yuri Reis Casal1,e, Jane Lucas4,5,f, Laura Behan4,5,6,g

Escola Bahiana de Medicina e Saúde

Pública, Salvador (BA) Brasil.

2. Divisão de Pneumologia, Instituto do

Coração – InCor – Hospital das Clínicas,

Faculdade de Medicina, Universidade

de São Paulo, São Paulo (SP) Brasil.

3. Departamento de Patologia, Faculdade

de Medicina, Universidade de

São Paulo, São Paulo (SP) Brasil.

4. Primary Ciliary Dyskinesia Centre, NIHR

Biomedical Research Centre, University

of Southampton, Southampton,

United Kingdom.

5. University Hospital Southampton NHS

Foundation Trust, Southampton,

United Kingdom.

6. School of Applied Psychology,

University College Cork, Cork, Ireland.

 

RESUMO

Primary ciliary dyskinesia (PCD) is a genetic disorder that is typically inherited in an

autosomal recessive manner. It is clinically characterized by recurrent respiratory

infections. However, its repercussions for patient quality of life should not be overlooked.

Studies have shown that PCD has a significant impact on the lives of patients, although

there are as yet no PCD-specific markers of quality of life. To address that problem,

researchers in the United Kingdom developed a quality-of-life questionnaire for patients

with PCD. The present communication focuses on the process of translating that

questionnaire into Brazilian Portuguese, through a partnership between researchers in

Brazil and those in the United Kingdom, as well as its subsequent application in patients

in Brazil.

 

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