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    Alpha1 Association of Australia

  • 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...

  • 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...

  • 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...

  • 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...

  • 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...

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