Wilson Disease and Alpha1-Antitrypsin Deficiency: A Review of Non-Invasive Diagnostic Tests

Wilson disease and alpha1-antitrypsin deficiency are two rare genetic diseases that may impact predominantly the liver and/or the brain, and the liver and/or the lung, respectively. The early diagnosis of these diseases is important in order to initiate a specific treatment, when available, ideally...

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Detalles Bibliográficos
Autores principales: Guillaud, Olivier, Dumortier, Jérôme, Couchonnal-Bedoya, Eduardo, Ruiz, Mathias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9857715/
https://www.ncbi.nlm.nih.gov/pubmed/36673066
http://dx.doi.org/10.3390/diagnostics13020256

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9857715/
https://www.ncbi.nlm.nih.gov/pubmed/36673066
http://dx.doi.org/10.3390/diagnostics13020256

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