Recommendations for the diagnosis and treatment of alpha-1 antitrypsin deficiency

Recommendations for the diagnosis and treatment of alpha-1 antitrypsin deficiency

ABSTRACT Alpha-1 antitrypsin deficiency (AATD) is a relatively rare genetic disorder, inherited in an autosomal codominant manner, that results in reduced serum AAT concentrations, with a consequent reduction in antielastase activity in the lungs, as well as an increased risk of diseases such as pul...

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Bibliographic Details
Main Authors: Paulo Henrique Ramos Feitosa, Maria Vera Cruz de Oliveira Castellano, Claudia Henrique da Costa, Amanda da Rocha Oliveira Cardoso, Luiz Fernando Ferreira Pereira, Frederico Leon Arrabal Fernandes, Fábio Marcelo Costa, Manuela Brisot Felisbino, Alina Faria França de Oliveira, Jose R Jardim, Marc Miravitlles
Format: Article
Language:English
Published: Sociedade Brasileira de Pneumologia e Tisiologia 2024-12-01
Series:Jornal Brasileiro de Pneumologia
Subjects:
alpha 1-antitrypsin
Emphysema
Pulmonary disease, chronic obstructive
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1806-37132024000500700&lng=en&tlng=en
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