Fulminant hepatic failure in the setting of progressive ANCA-associated vasculitis associated with a rare alpha-1 antitrypsin phenotype, ’PiEE'

Abnormalities in alpha-1 antitrypsin (AAT) proteins are risk factors for human disease. While the most common is AAT deficiency, a genetic disorder associated with chronic obstructive pulmonary disease, additional disorders associated with AAT abnormalities are increasingly recognised. We describe a...

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Detalles Bibliográficos
Autores principales: Reilkoff, Ronald, Stephenson, Laurel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2018
Materias:
Unusual Association of Diseases/Symptoms
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5878378/
https://www.ncbi.nlm.nih.gov/pubmed/29592975
http://dx.doi.org/10.1136/bcr-2017-222036

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5878378/
https://www.ncbi.nlm.nih.gov/pubmed/29592975
http://dx.doi.org/10.1136/bcr-2017-222036

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