Zerres K
Institut für Humangenetik der Universität Bonn, Federal Republic of Germany.
Pediatr Nephrol. 1987 Jul;1(3):397-404. doi: 10.1007/BF00849243.
Despite the high incidence of cystic kidney diseases, affected families are not usually well informed of the inheritance of these disorders. Genetic counselling must be based on precise diagnostic criteria. Detailed information on the different types of cystic kidney disease is summarized, including clinical features, pathology, radiology, prenatal diagnosis and the risk of recurrence. In addition, a genetic interpretation is given of the Caroli syndrome, Potter sequence as well as congenital hepatic fibrosis.
尽管囊性肾病发病率很高,但患病家庭通常对这些疾病的遗传情况了解不足。遗传咨询必须基于精确的诊断标准。本文总结了不同类型囊性肾病的详细信息,包括临床特征、病理学、放射学、产前诊断及复发风险。此外,还对卡罗利综合征、波特序列征以及先天性肝纤维化进行了遗传学解读。