Alpha-1 antitrypsin (an-tee-TRIP-sin) deficiency, or AAT deficiency, is a condition that raises your risk for lung disease (especially if you smoke) and other diseases.
WebMD explains the causes, symptoms, and treatment of Alpha-1 antitrypsin deficiency, a disease passed down from your parents that can make it hard to breathe.
Alpha-1 antitrypsin deficiency is an inherited disorder that may cause lung disease and liver disease. The signs and symptoms of the condition and the age ...
Learn about Alpha-1 Antitrypsin Deficiency (A-1ATD), an inherited condition that causes lung and liver disease in adults.
What is Alpha-1? Top Alpha-1 News stories. Alpha-1 Number 1 Goal - Find a cure for Alpha-1 Deficiency. Research, Advocacy, and Support Groups.
Alpha 1-antitrypsin deficiency (α1-antitrypsin deficiency, A1AD) is a genetic disorder that causes defective production of alpha 1-antitrypsin (A1AT), leading to ...
What is Alpha-1 Antitrypsin Deficiency? Alpha-1 antitrypsin deficiency (Alpha-1) is a hereditary genetic disorder which may lead to the development of lung and/or ...
Alpha-1 antitrypsin (AAT) deficiency is a condition in which the body does not make enough of a protein that protects the lungs and liver from damage.
It is possible that the main title of the report Alpha-1 Antitrypsin Deficiency is not the name you expected. Please check the synonyms listing to find the ...
What is Alpha-1? Alpha-1 Antitrypsin Deficiency (Alpha-1) is a genetic (inherited) condition – it is passed from parents to their children through their genes.