Prenatal MR imaging features of Caroli syndrome in association with autosomal recessive polycystic kidney disease

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 in postnatal ultrasound, the diagnosis of Caroli...

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Detalles Bibliográficos
Autores principales: Rivas, Amanda, Epelman, Monica, Danzer, Enrico, Adzick, N. Scott, Victoria, Teresa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Pediatric
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6260464/
https://www.ncbi.nlm.nih.gov/pubmed/30510609
http://dx.doi.org/10.1016/j.radcr.2018.11.006

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6260464/
https://www.ncbi.nlm.nih.gov/pubmed/30510609
http://dx.doi.org/10.1016/j.radcr.2018.11.006

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