Affiliation:
1. Department of Pathology and Nuffield Department of Child Health, The Queen's University, Belfast, and The Royal Belfast Hospital for Sick Children, Belfast, North Ireland
Abstract
The typical clinical features of uremic medullary cystic disease—anemia, polyuria, polydypsia, and uremia—were observed in three young siblings (the typical setting of familial juvenile nephronophthisis). Renal juxtemedullary cysts were found at autopsy in one sibling, confirming the concept that these two diseases are truly rehated. The mother of the siblings studied in this paper demonstrated an inability to concentrate urine.
Publisher
American Academy of Pediatrics (AAP)
Subject
Pediatrics, Perinatology, and Child Health
Cited by
1 articles.
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