Imaging manifestations of Caroli disease with autosomal recessive polycystic kidney disease: a case report and literature review

• Príomhchruthaitheoirí: Xiuzhen Yao (Údar), Weiqun Ao (Údar), Jianhua Fang (Údar), Guoqun Mao (Údar), Chuanghua Chen (Údar), Lifang Yu (Údar), Huaijie Cai (Údar), Chenke Xu (Údar)
• Formáid: LEABHAR
• Foilsithe / Cruthaithe: BMC, 2021-04-01T00:00:00Z.
• Ábhair: article
• Rochtain ar líne: Connect to this object online.

Abstract Background Both Caroli disease (CD) and autosomal recessive polycystic kidney disease (ARPKD) are autosomal recessive disorders, which are more commonly found in infants and children, for whom surviving to adulthood is rare. Early diagnosis and intervention can improve the survival rate to...