Alpha1 Awareness provides information, advice and support for people who are affected by Alpha-1 Antitrypsin Deficiency.
Alpha1 antitrypsin deficiency is a genetic defect on chromosome 14 that causes the liver either not to produce the protein called alpha1 antitrypsin (AAT) or to produce this substance with errors in the structure of its molecules. These badly formed molecules fold incorrectly and become, by and large, unable to leave the liver.
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Who to contact
Where to go
- Alpha 1 Awareness
PO Box 2866
- BS5 5EE