Explore Treatments for Alpha-1 Antitrypsin (A1AT) Deficiency

Alpha-1 antitrypsin (A1AT) deficiency is a rare, long-term illness caused by an inherited abnormal gene mutation that primarily affects the lungs and liver. People with this condition are more likely to develop lung diseases like emphysema and liver problems such as cirrhosis. Common symptoms include liver disease, shortness of breath, chronic cough and extreme tiredness. A1AT deficiency affects about 1 in every 3,500 people. There is no cure, but early detection and proper care can help manage the condition and improve quality of life.