Oct 18, 2022 · Alpha-1 antitrypsin deficiency (sometimes just called “Alpha-1”) is an inherited genetic disorder that causes low levels of a protein (AAT) that protects your lungs.

Nov 25, 2025 · Alpha-1 is a rare disease that makes an enzyme in your liver work poorly. Alpha-1 antitrypsin protein usually travels from your liver through your blood to protect your lungs and other...

Alpha-1 Antitrypsin Deficiency (Alpha-1) is a genetic condition that can cause damage to the lungs and/or the liver. There is no cure for Alpha-1, but some symptoms can be managed with treatment.

Apart from COPD and chronic liver disease, α 1 -antitrypsin deficiency has been associated with necrotizing panniculitis (a skin condition) and with granulomatosis with polyangiitis in which …

Mar 12, 2025 · Alpha-1 antitrypsin (AAT) deficiency puts you at greater risk for lung, liver or skin disease. AAT is normally produced in the liver and travels through the blood to protect the lungs and …

Alpha-1 antitrypsin deficiency occurs worldwide, but its prevalence varies by population. This disorder affects about 1 in 1,500 to 3,500 individuals with European ancestry. It is uncommon in people of …

Alpha-1 Antitrypsin Deficiency (Alpha-1) is a genetic (inherited) condition that is passed from parents to their children through their genes. Alpha-1 may result in serious lung disease in adults and/or liver …

What Is Alpha-1? Alpha-1 Antitrypsin Deficiency (Alpha-1) is a hereditary condition that is passed on from parents to their childr. n through genes. This condition may result in serious lung disease in …

Alpha-one antitrypsin deficiency is an inherited condition. Every person inherits two AAT genes—one from each parent. Inheriting two abnormal AAT genes causes very low levels of AAT in the blood. A …

From its genetic nature to its associated symptoms and risk factors, we've got you covered when it comes to learning more about Alpha‑1 antitrypsin deficiency (Alpha‑1, for short).