SOCIAL QUESTIONS|health|illness
- uireasa antaitripsin alfa-1 Reference Faomhadh an téarma seo mar chuid de Thionscadal Lex
- ga
- Laurell-Eriksson-Syndrom | α1-Antitrypsinmangel | Alpha-1-Antitrypsinmangel | AAT-Defizit | Proteaseinhibitormangel
- de
- Definition erbliche Stoffwechselerkrankung aufgrund eines Polymorphismus des Proteinase-Systems Reference Wikipedia, http://de.wikipedia.org/wiki/Alpha-1-Antitrypsinmangel (14.3.2008)
- AAD | A1AD | AAT | Alpha-1-Antitrypsin Deficiency | AATD | α1-antitrypsin deficiency
- en
- Definition genetic disorder that manifests as pulmonary emphysema, liver cirrhosis and, rarely, as the skin disease panniculitis, and is characterized by low serum levels of AAT, the main protease inhibitor (PI) in human serum Reference ORPHANET > Alpha-1 antitrypsin deficiency, http://www.orpha.net/consor/cgi-bin/Disease_Search.php?lng=EN&data_id=194&Disease_Disease_Search_diseaseGroup=alpha-deficiency&Disease_Disease_Search_diseaseType=Pat&Disease(s)%20concerned=Alpha-1-antitrypsin-deficiency&title=Alpha-1-antitrypsin-deficiency&search=Disease_Search_Simple (15.6.2009)