Défice de alfa-1 antitripsina. A propósito de dois casos clínicos

AbstractThe alpha-1 antitrypsin deficiency is an hereditary autosomic codominant disease. The phenotype Pi ZZ is associated more frequently with pulmonary disease and is responsible for the presence of emphysema early in life, particularly in smokers. The author’s present two cases which diagnosis were performed later in life and in which other factors could be also responsible for clinical manifestations.Rev Port Pneumol 2007; XIV (2): 295-30