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Expert Perspectives on the Management of Alpha 1-Antitrypsin Deficiency

Conde, Bebiana; Costa, Filipa; Gomes, Joana; Lopes, António Paulo; Mineiro, Maria Alexandra; Rodrigues, Orlando; Santos, Cristina; Semedo, Luísa

Alpha 1-antitrypsin deficiency is an inherited autosomal codominant disorder, which predisposes patients to lung and/or liver disease. Even though it is considered rare, it is one of the most frequent genetic disorders worldwide, albeit remaining underdiagnosed. Several organizations and societies, including the Portuguese Society of Pulmonology have been elaborating guidelines and recommendations for the diagn...

Date: 2022   |   Origin: Acta Médica Portuguesa
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