Una causa tratable de EPOC | 05 DIC 16

Deficiencia de Alfa-1 Antitripsina

Es un trastorno genético común pero subdiagnosticado, que aumenta el riesgo de EPOC y enfermedad hepática.
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REFERENCIAS

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12. Campos M, Hagenlocker B, Martinez N, et al. Impact of an electronic medical record clinical reminder to improve detection of COPD and alpha-1 antitrypsin deficiency in the Veterans Administration (VA) system (abstract). Am J Respir Crit Care Med 2011; 183:A5356.

www.atsjournals.org/doi/pdf/10.1164/ajrccm-conference.2011.183.1_MeetingAbstracts

A5356. Accessed May 24, 2016.

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18. McElvaney NG, Stoller JK, Buist AS, et al. Baseline characteristics of enrollees in the National Heart, Lung and Blood Institute Registry of Alpha 1-Antitrypsin Deficiency. Alpha 1-Antitrypsin Deficiency Registry Study Group. Chest 1997; 111: 394–403.

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