Alpha1-antitrypsin (A1AT) deficiency is a relatively

Alpha1-antitrypsin (A1AT) deficiency is a relatively

Physiology homework help Alpha1-antitrypsin (A1AT) deficiency is a relatively rare genetic disorder that causes affected individuals to have a predisposition to developing early signs of chronic obstructive pulmonary disorder (COPD), non-alcoholic cirrhosis of the liver, and in some cases, a skin disease called panniculitis. The most common cause of mortality in individuals with A1AT deficiency […]