多囊性肾病
肝硬化
医学
多囊肾病
多囊性疾病
肾
先天性肝纤维化
多囊肾
多囊性肝病
疾病
病理
肝病
病因学
肾脏疾病
常染色体显性多囊肾病
胃肠病学
内科学
出处
期刊:PubMed
日期:2016-10-20
卷期号:24 (10): 728-731
被引量:2
标识
DOI:10.3760/cma.j.issn.1007-3418.2016.10.003
摘要
There are two common types of hereditary polycystic kidney diseases, autosomal dominant polycystic kidney disease and autosomal recessive polycystic kidney disease. Congenital hepatic fibrosis is an autosomal recessive disorder and can occur in hereditary polycystic kidney disease. Therefore, hereditary polycystic kidney disease is one of the causes of unexplained liver fibrosis and liver cirrhosis.
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