Alpha-1 Antitrypsin Deficiency
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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.
This video in 30 seconds
This video explains alpha-1 antitrypsin deficiency, a genetic inherited condition passed from parents to children through their genes. It covers that alpha-1 may result in serious lung disease in adults and/or liver disease at any age.
Key points
- Defines alpha-1 antitrypsin deficiency as an inherited genetic condition
- Covers serious lung disease in adults as a possible result
- Covers liver disease at any age as a possible result
Video Overview
This video presents “Alpha-1 Antitrypsin Deficiency” — 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. Whether you are preparing for a procedure, studying the technique, or learning how a condition is assessed, the recording shows the process as it is performed in practice.
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