Déficit de Alfa-1-antitripsina y su tratamiento
Alpha-1 antitrypsin deficiency and its treatment
Rev. Hosp. Clin. Univ. Chile; 28 (3), 2017
Alpha-1 antitrypsin deficiency (AATD) is a genetic disorder caused by a mutation in the codifying
gene for the alpha-1 antitrypsin (AAT) protein, which has anti-elastase activity. While there is
extensive genetic variability, the most common genotypes associated with AATD are PI*Z y
PI*S. Most clinical m...