Familial Juvenile Nephronophthisis: A Review and Differential Diagnosis

Arnaldo Cantani*, Gabriele Bamonte, Daniel Ceccoli, Gianni Biribicchi, Francesco Farinella

*Corresponding author for this work

Research output: Contribution to journalLiterature reviewpeer-review

Abstract

Familial juvenile nephronophthisis (FJN) is a frequent cause of chronic renal failure in children and adolescents. Typically it presents after 6 years of age through adolescence, but may become apparent in early childhood. The clinical presentation is insidious, and the early symptoms of polyuria and polydipsia are often overlooked in the presence of a relatively normal urinalysis and in the absence of proteinuria, azotemia, and hypertension. Thus most patients are not diagnosed until after the onset of renal failure. These children are excellent candidates for properly selected transplantation.
Original languageAmerican English
Pages (from-to)90-95
Number of pages6
JournalClinical Pediatrics
Volume25
Issue number2
DOIs
StatePublished - Feb 1986
Externally publishedYes

ASJC Scopus Subject Areas

  • Pediatrics, Perinatology, and Child Health

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