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pro vyhledávání: '"Amanda Rivas"'
Autor:
Amanda Rivas, Monica Epelman, MD, Enrico Danzer, MD, N. Scott Adzick, MD, Teresa Victoria, MD, PhD
Publikováno v:
Radiology Case Reports, Vol 14, Iss 2, Pp 265-268 (2019)
Caroli syndrome, which is characterized by saccular and fusiform dilatation of the biliary ducts, is usually observed in association with autosomal recessive polycystic kidney disease (ARPKD). Although the diagnosis of ARPKD is generally easy to make
Externí odkaz:
https://doaj.org/article/07d5122be15b41ab97b3205aeebc2220
Publikováno v:
Radiology Case Reports
Radiology Case Reports, Vol 14, Iss 2, Pp 265-268 (2019)
Radiology Case Reports, Vol 14, Iss 2, Pp 265-268 (2019)
Caroli syndrome, which is characterized by saccular and fusiform dilatation of the biliary ducts, is usually observed in association with autosomal recessive polycystic kidney disease (ARPKD). Although the diagnosis of ARPKD is generally easy to make