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Improving the Lives of Patients with Alpha-1 Antitrypsin Deficiency
Alpha-1 Antitrypsin Deficiency (AATD) is a rare genetic condition that predisposes patients to lung and liver disease and is often underdiagnosed due to incomplete diagnosis of chronic obstructive pulmonary disease (COPD) and asthma. Improvements in physician awareness have been made, but better str...
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| Publicado no: | Int J Chron Obstruct Pulmon Dis |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Dove
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7735792/ https://ncbi.nlm.nih.gov/pubmed/33328731 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/COPD.S276773 |
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