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1" in Liapis and Winyard (121)) and offers additional tables that display entities within the differential diagnosis of glomerulocystic kidney disease and the developmental defects within the CAKUT spectrum and a lengthy tabulation of many genetic syndromes complicated by CAKUT (see Table 26.
14,26) Molecular genetics has demonstrated that there is an autosomal dominant type of familial glomerulocystic kidney disease (ADGCKD), which is distinct from autosomal dominant and autosomal recessive polycystic kidney diseases (PKDs).