alpha-1 antitrypsin deficiency
Type: Concept
As of November 2026, alpha-1 antitrypsin deficiency has been mentioned in one podcast episode on Osmosis from Elsevier (Jan 2026).
A genetic disorder caused by mutations in the SERPINA1 gene, leading to lung and liver disease.
| Mentioned in | 1 episode on 1 podcast (as of November 2026) |
|---|---|
| First heard | Jan 2026 on Osmosis from Elsevier |
Who talks about alpha-1 antitrypsin deficiency on podcasts?
alpha-1 antitrypsin deficiency came up; the most recent mention was Jan 2026 on Osmosis from Elsevier.
What is alpha-1 antitrypsin deficiency mentioned alongside?
alpha-1 antitrypsin deficiency is most often mentioned alongside primary ciliary dyskinesia, Marfan syndrome and Cartagena syndrome.
Mentioned together: primary ciliary dyskinesia, Marfan syndrome, Cartagena syndrome, FBN1