Alpha-1-antitrypsin deficiency


What is Alpha-1 antitrypsin deficiency?

Alpha-1 antitrypsin deficiency (AATD) is an inherited condition, caused by changes, or mutations, in the SERPINA1 gene, that can lead to lung disease and liver disease. There is a strong risk factor for emphysema in particular, and AATD is a common known genetic risk factor for this. It is caused by low levels of alpha-1 antitrypsin in the blood, which is a protein made in the liver that usually protects the lungs.

Alpha-1 Foundation. Retrieved August 28, 2017 from

CHEST Foundation. Retrieved from

This content comes from a hidden element on this page.

The inline option preserves bound JavaScript events and changes, and it puts the content back where it came from when it is closed.

Remember Me