Alpha-1 Antitrypsin Deficiency or Alpha-1 is a genetic (inherited) condition that may result in serious, chronic lung and/or liver disease at various ages in life (children and adults). Disease is caused by an abnormal alpha1 protein that is mainly produced by the liver.

Although Alpha-1 is one of the most common genetic disorders in the world, it is often misdiagnosed. Many times patients are told they have asthma, bronchitis, symptoms related to stress, emphysema caused by smoking, or simply chronic obstructive pulmonary disease of unknown cause.

The most common indicators of Alpha-1 include shortness of breath, a chronic cough, and abnormal liver test results. If you have any of these symptoms there is a simple blood test that can detect alpha-1 antitrypsin levels.

Despite treatments, including protein replacement, adults may require a lung transplant due to severe emphysema.

Visit the Alpha-1 website for more information and find out ways you can help raise awareness of Alpha-1!