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Alpha-1 antitrypsin deficiency: an update on clinical aspects of diagnosis and management
Clinical heterogeneity has been demonstrated in alpha-1 antitrypsin deficiency (AATD), such that clinical suspicion plays an important role in its diagnosis. The PiZZ genotype is the most common severe deficiency genotype and so tends to result in the worst clinical presentation, hence it has been t...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Faculty Opinions Ltd
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7886062/ https://www.ncbi.nlm.nih.gov/pubmed/33659933 http://dx.doi.org/10.12703/b/9-1 |