ABCB4 gene mutation-associated cirrhosis with systemic amyloidosis: A case report

BACKGROUND: Gene mutations in ATP-binding cassette, subfamily B (ABCB4) lead to autosomal recessive disorders. Primary light amyloidosis is a rare and incurable disease. Here, we report a rare case of liver cirrhosis caused by ABCB4 gene mutation combined with primary light amyloidosis. CASE SUMMARY...

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Detalles Bibliográficos
Autores principales: Cheng, Na, Qin, Yu-Jie, Zhang, Quan, Li, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10424036/
https://www.ncbi.nlm.nih.gov/pubmed/37584002
http://dx.doi.org/10.12998/wjcc.v11.i20.4903

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10424036/
https://www.ncbi.nlm.nih.gov/pubmed/37584002
http://dx.doi.org/10.12998/wjcc.v11.i20.4903

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