TY - JOUR T1 - GPs Meet Rare Lung Disorders Task Force factsheet: α-1 antitrypsin deficiency JF - Breathe JO - Breathe SP - 87 LP - 89 DO - 10.1183/20734735.000414 VL - 10 IS - 1 AU - Bruno Balbi Y1 - 2014/03/01 UR - http://breathe.ersjournals.com/content/10/1/87.abstract N2 - Definition α-1 antitrypsin deficiency (AATD) is a genetic disorder that manifests as pulmonary emphysema, liver cirrhosis and, rarely, as the skin disease panniculitis, or as vasculitis and is characterised by low serum levels of AAT, the main protease inhibitor in human serum. Key messages Think about AATD if your patient had emphysema at younger age. Assess the levels of blood AAT to ascertain the diagnosis by the finding of reduced levels. Refer the patient to a Department with experience in lung/liver manifestations of AATD. Follow the patient longitudinally in collaboration with the reference center. Issues to consider are replacement therapy (if needed or available) and clinical evolution toward respiratory or liver failure. ER -