Congenital hepatic fibrosis and adult-type autosomal dominant polycystic kidney disease in a child
- 1 July 1985
- journal article
- case report
- Published by Oxford University Press (OUP)
- Vol. 61 (717) , 641-642
- https://doi.org/10.1136/pgmj.61.717.641
Abstract
Summary: This reports a family with congenital hepatic fibrosis and adult polycystic kidney disease. Adult polycystic kidney disease was present in three generations. In addition, congenital hepatic fibrosis occurred in two members of the third generation. These conditions are generally held to have different modes of inheritance and the significance of their occurrence together is not clear.Keywords
This publication has 8 references indexed in Scilit:
- Congenital Hepatic Fibrosis and Asymptomatic Familial Adult-Type Polycystic Kidney Disease in a 19-Year-Old WomanGastroenterology, 1984
- Kidney Polycystic Disease in Adult Congenital Hepatic FibrosisAnnals of Internal Medicine, 1978
- Congenital Hepatic Fibrosis-Is it a Single Clinical Entity?Gastroenterology, 1973
- Congenital hepatic fibrosis: report of two new cases and review of the literature.1973
- Polycystic disease of kidney and liver presenting in childhood.Journal of Medical Genetics, 1971
- INFANTILE POLYCYSTIC DISEASE OF THE KIDNEYS AND LIVERMedicine, 1971
- Congenital polycystic disease of kidneys and liver. Portal hypertension--portacaval anastomosis.1968
- Congenital hepatic fibrosis.1961