Heterozygous Alpha-1 Antitrypsin Deficiency Causing Pulmonary Emboli and Pulmonary Bullae

Alpha-1 antitrypsin deficiency is an autosomal co-dominant disease known for different genetic alterations in the serine protease inhibitor enzyme by which different disease phenotypes can manifest. The lung and the liver are the most common organs involved. The severity of the disease depends on th...

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Detalles Bibliográficos
Autores principales: Tannous, Toufic, Rosso, Claudia, Keating, Matthew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8164444/
https://www.ncbi.nlm.nih.gov/pubmed/34084683
http://dx.doi.org/10.7759/cureus.14759

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8164444/
https://www.ncbi.nlm.nih.gov/pubmed/34084683
http://dx.doi.org/10.7759/cureus.14759

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