Objective: To investigate whether implementation of a coeliac disease (CD)-specific health related quality of life (HRQOL) questionnaire would add value to CD follow-up visits; we compared patients' self-reported CD-specific HRQOL with the physician's report provided during a regular CD follow-up visit in children and young adults. Methods: A cross-sectional study in the control group of a study on self-management in CD (CoelKids). Eligible patients had CD for >=1year and were
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