Literature DB >> 3449470

Infantile nephronophthisis.

E Bodaghi1, M T Honarmand, M Ahmadi.   

Abstract

Juvenile nephronophthisis is a common cause of end stage renal failure in children and adolescents. The early occurrence with rapid progression to advanced renal failure has not previously been described. In this report we present three babies in whom failure to thrive, dehydration and a renal concentrating defect presented soon after birth; they were subsequently investigated for renal failure during the first year of life. In two cases the association with congenital hepatic fibrosis was noted. A family history of nephronophthisis was not present but the parents were consanguineous and one sibling had died in infancy.

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Year:  1987        PMID: 3449470

Source DB:  PubMed          Journal:  Int J Pediatr Nephrol        ISSN: 0391-6510


  3 in total

1.  Identification of a new gene locus for adolescent nephronophthisis, on chromosome 3q22 in a large Venezuelan pedigree.

Authors:  H Omran; C Fernandez; M Jung; K Häffner; B Fargier; A Villaquiran; R Waldherr; N Gretz; M Brandis; F Rüschendorf; A Reis; F Hildebrandt
Journal:  Am J Hum Genet       Date:  2000-01       Impact factor: 11.025

2.  Does liver biopsy provide sufficient diagnostic information to differentiate autosomal recessive from autosomal dominant polycystic kidney disease?

Authors:  B R Cole
Journal:  Pediatr Nephrol       Date:  1994-08       Impact factor: 3.714

3.  Infantile chronic tubulo-interstitial nephritis with cortical microcysts: variant of nephronophthisis or new disease entity?

Authors:  M F Gagnadoux; J L Bacri; M Broyer; R Habib
Journal:  Pediatr Nephrol       Date:  1989-01       Impact factor: 3.714

  3 in total

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