Expert Perspectives on the Management of Alpha 1-Antitrypsin Deficiency

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,...

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Библиографические подробности
Главные авторы: Bebiana Conde, Filipa Costa, Joana Gomes, António Paulo Lopes, Maria Alexandra Mineiro, Orlando Rodrigues, Cristina Santos, Luísa Semedo, Maria Sucena, Catarina Guimarães
Формат: Статья
Язык:English
Опубликовано: Ordem dos Médicos 2022-07-01
Серии:Acta Médica Portuguesa
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Online-ссылка:https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/18497