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Pharma & Healthcare

Alpha 1 Antitrypsin Deficiency Treatment

Alpha-1 antitrypsin deficiency (A1AD) is a hereditary disorder characterized by low levels of a protein called alpha-1 antitrypsin (A1AT) which is found in the blood. This deficiency may predispose an individual to several illnesses and most commonly manifests as chronic obstructive pulmonary disease (including bronchiectasis) and liver disease (especially cirrhosis and hepatoma), or more rarely, as a skin condition called panniculitis. A1AD is also more frequent among…

Types
Augmentation Therapy · Cystic Fibrosis(CF) · Non-CF Bronchiectasis(NCFB)
Applications
COPD · Cystic Fibrosis(CF) · Non-CF Bronchiectasis(NCFB)

5 editions29 December 2025

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