Incidental alpha-1-antitrypsin deficiency found in post-transplant liver allografts: Report of two cases

Alpha-1 antitrypsin deficiency is an autosomal recessive disease most commonly caused by misfolding of the Alpha-1-antitrypsin protein, which prevents its release from hepatocytes into the systemic circulation. This results in increased lifetime risk of liver and lung disease. Due to its variable pe...

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Detalles Bibliográficos
Autores principales: Lee, Jonathan, Yoshida, Eric M., Mattman, Andre, Marquez, Vladimir, Bukhari, Hussam, Farnell, David, Yang, Hui-Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kare Publishing 2021
Materias:
Case Report - Alpha-1-antitrypsin deficiency in liver allografts
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9138925/
https://www.ncbi.nlm.nih.gov/pubmed/35782889
http://dx.doi.org/10.14744/hf.2020.2020.0013

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9138925/
https://www.ncbi.nlm.nih.gov/pubmed/35782889
http://dx.doi.org/10.14744/hf.2020.2020.0013

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