SOCIAL QUESTIONS|health|illness
- uireasa antaitripsin alfa-1 Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
- ga
- Laurell-Eriksson-Syndrom | α1-Antitrypsinmangel | Alpha-1-Antitrypsinmangel | AAT-Defizit | Proteaseinhibitormangel
- de
- Sainmhíniú erbliche Stoffwechselerkrankung aufgrund eines Polymorphismus des Proteinase-Systems Tagairt Wikipedia, http://de.wikipedia.org/wiki/Alpha-1-Antitrypsinmangel (14.3.2008)
- AAD | A1AD | AAT | Alpha-1-Antitrypsin Deficiency | AATD | α1-antitrypsin deficiency
- en
- Sainmhíniú 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 Tagairt 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)