Alpha-1 antitrypsin (A1AT) deficiency is a co-dominant genetic disorder, with dyspnoea and a chronic cough. The lack of A1AT enables neutrophil elastase to break down elastin in the lungs causing emphysema which especially affects the lower lobes. Tram-track lines suggest bronchiectasis. A1AT is often mistaken for asthma. In some forms (e.g. the PiMZ genotype, his mother is well - PiMM, and father is ill - PiZZ) symptoms are precipitated/exacerbated by environmental insults (smoking, dust inhalation). Emphysema is secondary, implied by age 35, family history, and only 2 pack-years of smoking.