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AAA
Please consider visiting the web sites of our valued sponsors. Let them know that the AAA referred you, which tells our sponsors that we appreciate their support. If you’re feeling cashed up, please ...
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What is Alpha-1? – AAA
Alpha-1 Antitrypsin Deficiency (Alpha-1) is a condition that is passed on from parents to their children through genes. This condition may result in serious lung and/or liver disease at various ages i...
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Alpha-1 Lung Disease – AAA
AATD Lung Disease Alpha-1 Antitrypsin (AAT) protects the delicate tissues of the lungs by binding to neutrophil elastase, a protein released by white blood cells which digests bacteria and other forei...
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Information – AAA
Alpha-1 Antitrypsin Deficiency (AATD), sometimes referred to as Alpha-1, is a genetic (inherited) condition that may result in serious, chronic lung and/or liver disease at various ages in life (child...
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Panniculitis in Alpha-1 – AAA
The following article is a reprint from the Alpha-1 Foundation Research Registry Update Spring/Summer Issue 2007. See also Alpha-1 Foundation > Newly Diagnosed > Learning About AATD > Panniculitis. Pa...
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How is Alpha-1 Diagnosed? – AAA
Although Alpha-1 Antitrypsin Deficiency (AATD) 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 r...