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Alpha-1 Antitrypsin Deficiency as related to Albuterol


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

 

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.

Salbutamol (INN) or albuterol (USAN) is a short-acting β2-adrenergic receptor agonist used for the relief of bronchospasm in conditions such as asthma and COPD. It is marketed by the Allen & Hanbury's respiratory division of GlaxoSmithKline under the trade name Ventolin. The name Albuterol comes from Salbutamol aersol.


Alpha-1 Antitrypsin Deficiency as related to Albuterol


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November 23, 2009


Page Updated: January 17, 2009
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