Abernethy malformation associated with Caroli’s syndrome in a patient with a PKHD1 mutation: a case report

Abernethy malformation associated with Caroli’s syndrome in a patient with a PKHD1 mutation: a case report

Abstract Background Abernethy malformation is a rare congenital anomaly characterised by the partial or complete absence of the portal vein and the subsequent development of an extrahepatic portosystemic shunt. Caroli’s disease is a rare congenital condition characterised by non-obstructive saccular...

Full description

Bibliographic Details
Main Authors: Xiao-xiao Mi, Xiao-guang Li, Zi-rong Wang, Ling Lin, Chun-hai Xu, Jun-ping Shi
Format: Article
Language:English
Published: BMC 2017-08-01
Series:Diagnostic Pathology
Subjects:
Abernethy malformation
Caroli’s syndrome
Liver biopsy
PKHD1
Online Access:http://link.springer.com/article/10.1186/s13000-017-0647-y

Similar Items

Similar Items