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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Detalles Bibliográficos
Autores principales: Renduchintala, Kavita, Pabbathi, Smitha, Nanjappa, Sowmya, Ramsakal, Asha, Greene, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2020
Materias:
Internal Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7805524/
https://www.ncbi.nlm.nih.gov/pubmed/33489496
http://dx.doi.org/10.7759/cureus.12078

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7805524/
https://www.ncbi.nlm.nih.gov/pubmed/33489496
http://dx.doi.org/10.7759/cureus.12078

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