Hypothesis
Author(s) -
Lawrence Copelovitch,
Martin A. Nash,
Bernard S. Kaplan
Publication year - 2007
Publication title -
clinical journal of the american society of nephrology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.755
H-Index - 151
eISSN - 1555-905X
pISSN - 1555-9041
DOI - 10.2215/cjn.00900207
Subject(s) - medicine , asymptomatic , proteinuria , nephrocalcinosis , hypercalciuria , focal segmental glomerulosclerosis , renal biopsy , disease , biopsy , pediatrics , urology , gastroenterology , urinary system , kidney
Dent disease is a hereditary form of progressive renal failure characterized by hypercalciuria and proximal tubular dysfunction. The clinical presentation is often insidious with the majority of patients remaining asymptomatic throughout childhood. Despite the seemingly mild, early course, more than 20% of 32 asymptomatic patients in one study had biopsy evidence of focal glomerulosclerosis. Furthermore, end-stage renal disease often occurs in men in early to middle adulthood.
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