{"title":"Renal Cystic Disease : Classification and Pathogenesis *","authors":"J. Bernstein","doi":"10.1111/j.1741-4520.1993.tb00507.x","DOIUrl":null,"url":null,"abstract":"Among the principal types of hereditary and developmental renal cystic disease (Table I), polycystic kidney disease (PKD) stands out because of its frequency and medical importance. The two principal categories of PKD are autosomal dominant (AD-PKD) and autosomal recessive (AR-PKD). Cystic kidney disease, often indistinguishable from classic PKD, is also inherent in several well-defined syndromes, among them tuberous sclerosis and von Hippel-Lindau disease.","PeriodicalId":93953,"journal":{"name":"Congenital anomalies","volume":"3 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"1993-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Congenital anomalies","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1111/j.1741-4520.1993.tb00507.x","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2
Abstract
Among the principal types of hereditary and developmental renal cystic disease (Table I), polycystic kidney disease (PKD) stands out because of its frequency and medical importance. The two principal categories of PKD are autosomal dominant (AD-PKD) and autosomal recessive (AR-PKD). Cystic kidney disease, often indistinguishable from classic PKD, is also inherent in several well-defined syndromes, among them tuberous sclerosis and von Hippel-Lindau disease.
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