Patient-centered assessment of treatment for alpha-1 antitrypsin deficiency: literature review to identify concepts and measures for people with alpha1-antitrypsin deficiency
Abstract Background Alpha-1 antitrypsin deficiency (AATD) is a genetic disorder that can result in a range of illnesses, with chronic obstructive pulmonary disease (COPD) being one of the most common. Although some people obtain genetic testing that identifies AATD, many people are unaware that they...
Main Authors: | Ekin Seçinti, Karolina Schantz, Laure Delbecque, John Krege, Rikki Mangrum, Sarah E. Curtis |
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Format: | Article |
Jezik: | English |
Izdano: |
BMC
2025-02-01
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Serija: | Orphanet Journal of Rare Diseases |
Teme: | |
Online dostop: | https://doi.org/10.1186/s13023-025-03592-9 |
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