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Alpha-1 Antitrypsin Deficiency Treatment and Symptoms


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Alpha-1 Antitrypsin Deficiency

AAT; alpha-1 proteinase inhibitor; alpha-1 related emphysema; genetic emphysema; hereditary pulmonary emphysema; inherited emphysema

Alpha-1 is an inherited disorder that may result in you developing a serious lung/ liver disease and passing the defective AAT gene onto your children. An estimated 100,000 people in the U.S. and a similar number in Europe are estimated to have the severe deficiency. In normal individuals large amounts of alpha-1 antitrypsin (AAT) is made in the liver and released into the blood. In AAT deficient individuals, the AAT made in the liver cannot be fully released into the blood.

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Alpha 1-antitrypsin deficiency (A1AD or Alpha-1) is a genetic disorder caus ...
Wikipedia - [full article]

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Alpha-1 Antitrypsin Deficiency Other

1-2 of 3   more...
Understanding Alpha-1 Antitrypsin Deficiency
... What is alpha-1 antitrypsin deficiency? Alpha-1 antitrypsin is a protein that is made in the liver. The liver releases this protein into the bloodstream. Alpha-1 antitrypsin protects the lungs so they...
Source: Cleveland Clinic

New Effort Seeks Increased Awareness of Lung Disorder
... A new initiative is underway to optimize the management of patients with a fairly common and potentially lethal lung disease known as alpha-1 antitrypsin disorder, or alpha-1. Part of the initiative i...
Source: Cleveland Clinic

   

Alpha-1 Antitrypsin Deficiency Articles

  • Alpha-1 antitrypsin deficiency
    ... Alpha-1 antitrypsin deficiency is an inherited disorder that can cause lung disease in adults and liver disease in adults and children. The first signs of lung disease caused by alpha-1 antitrypsin de...
    [full article...]



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May 13, 2008


Page Updated: October 3, 2005
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