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A Case of Alpha-1 Antitrypsin Deficiency and Organizing Pneumonia
Alpha-1 antitrypsin deficiency (AATD) is an autosomal dominant genetic disorder that presents with pulmonary complications and is most commonly manifested by panacinar emphysema and chronic obstructive pulmonary disease. A 49-year-old Caucasian female with a history of AATD and chronic tobacco use w...
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| Publicado no: | Cureus |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Cureus
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7805524/ https://ncbi.nlm.nih.gov/pubmed/33489496 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7759/cureus.12078 |
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