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Clinical characterization of a novel alpha1-antitrypsin null variant: PiQ0Heidelberg
oleh: Maria A. Presotto, Martina Veith, Frederik Trinkmann, Kai Schlamp, Markus Polke, Ralf Eberhardt, Felix Herth, Franziska C. Trudzinski
Format: | Article |
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Diterbitkan: | Elsevier 2022-01-01 |
Deskripsi
The clinical characterization of a null variant of SERPINA1 – PiQ0Heidelberg – resulting in alpha1-antitrypsin (AAT) deficiency is described. This rare mutation (c.-5+5 G > A) has been previously identified but not clinically described. The 77 year-old female patient had GOLD-3, Group B COPD, severe destructive panlobular emphysema and newly observed respiratory failure on exertion at the time the genetic analysis was performed. Serum AAT level was 0.1 g/L (reference 0.9–2.0 g/L). Isoelectric focusing showed only the Z-protein indicating that this was a null mutation. The patient has started AAT replacement. Early screening and identification of AAT deficiency would allow for earlier intervention.