Polycystic liver disease: Classification, diagnosis, treatment process, and clinical management

Polycystic liver disease (PLD) is a rare hereditary disease that independently exists in isolated PLD, or as an accompanying symptom of autosomal dominant polycystic kidney disease and autosomal recessive polycystic kidney disease with complicated mechanisms. PLD currently lacks a unified diagnostic...

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Detalles Bibliográficos
Autores principales: Zhang, Ze-Yu, Wang, Zhi-Ming, Huang, Yun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2020
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7097502/
https://www.ncbi.nlm.nih.gov/pubmed/32231761
http://dx.doi.org/10.4254/wjh.v12.i3.72

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7097502/
https://www.ncbi.nlm.nih.gov/pubmed/32231761
http://dx.doi.org/10.4254/wjh.v12.i3.72

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