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Alpha-1 Antitrypsin Deficiency (Alpha-1) is a genetic (inherited) condition – it is passed from parents to their children through their genes. Alpha-1 may result in serious lung disease in adults and/or liver disease at any age.
AATD or Alpha-1 Antitrypsin Deficiency is a lack of the protein alpha-1 antitrypsin (AAT) which is produced in the liver. The main job of AAT is to protect the lungs. A deficiency can lead to life-threatening lung and/or liver disease.
https://www.webmd.com/lung/copd/alpha-1-antitrypsin-deficiency-rare
Alpha-1 antitrypsin deficiency is a disease passed down from your parents that can make it hard to breathe. Find out about its causes, symptoms, diagnosis, and treatment.
https://www.cancertherapyadvisor.com/home/decision-support-in-medicine/pediatrics/alpha-1-antitrypsin-deficiency/
The possible outcomes of Alpha-1-Antitrypsin Deficiency are reviewed above and include chronic liver disease, chronic metabolic hepatitis, cirrhosis and liver cancer in children and adults, as ...
https://www.facebook.com/A1ADSupport/
Alpha-1 Antitrypsin Deficiency Support. 755 likes · 73 talking about this. This page is the public face of our closed community group for Alphas to learn, share, and find support after their diagnosis.5/5
https://www.dailystrength.org/group/alpha-1-antitrypsin-deficiency
Alpha-1 Antitrypsin Deficiency Support Group. Alpha 1-antitrypsin deficiency (A1AD or Alpha-1) is a genetic disorder caused by reduced levels of alpha 1-antitrypsin in the blood. It can lead to emphysema and, in some cases, to liver disease.
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