222 top medical experts on Autosomal Recessive alpha-1-Antitrypsin Deficiency across 22 countries and 19 U.S. states, including 68 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Autosomal Recessive alpha-1-Antitrypsin Deficiency: A rare hereditary, metabolic disease characterized by serum levels of alpha-1-antitrypsin (AAT) that are well below the normal range. In the most severe form, the disease can clinically manifest with chronic liver disorders (cirrhosis, fibrosis), respiratory disorders (emphysema, bronchiectasis), and rarely panniculitis or vasculitis.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Alpha-1 Protease Inhibitor Deficiency,  Alpha-1 Related Emphysema,  Genetic Emphysema,  Hereditary Pulmonary Emphysema,  Inherited Emphysema


  

        

                    


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