Alpha-1 Antitrypsin Deficiency: Principles of Care

Alpha-1 antitrypsin deficiency is an autosomal co-dominant inherited disorder that results in decreased circulating levels of alpha-1 antitrypsin (also known as alpha-1 proteinase inhibitor) and predisposes affected individuals to early onset lung and liver disease. There is currently no cure for al...

Full description

Bibliographic Details
Main Author: Rodrigues, Joana F. (author)
Other Authors: Mineiro, Alexandra (author), Reis, António (author), Ventura, David G. (author), Fernandez-Llimos, Fernando (author), Costa, Filipa (author), Gomes, Joana (author), Silva, José Manuel (author), Lopes, Paulo (author), Cordeiro, Carlos Robalo (author)
Format: article
Language:eng
Published: 2020
Subjects:
alpha 1-Antitrypsin Deficiency/therapy
Health Care Quality
Access
and Evaluation
Professional Practice
Standard of Care
Acesso e Avaliação dos Cuidados de Saúde
Deficiência de alfa 1–Antitripsina/tratamento
Padrão de Cuidado
Qualidade
Prática Profisional
Online Access:https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/12950
Country:Portugal
Oai:oai:ojs.www.actamedicaportuguesa.com:article/12950

Internet

https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/12950

Similar Items