Literature DB >> 9044325

Autosomal recessive polycystic kidney disease.

K Zerres1, S Rudnik-Schöneborn, C Steinkamm, G Mücher.   

Abstract

Autosomal recessive polycystic kidney disease (ARPKD) is a rare inherited disorder which usually becomes clinically manifest in early childhood. With increasing knowledge and improving diagnostic techniques it has become evident that the spectrum of ARPKD is much more variable than was previously thought. Presentation of ARPKD at later ages and survival into adulthood is well known. Diagnostic criteria, clinical course, genetics and differential diagnosis of ARPKD are presented.

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Year:  1996        PMID: 9044325     DOI: 10.1093/ndt/11.supp6.29

Source DB:  PubMed          Journal:  Nephrol Dial Transplant        ISSN: 0931-0509            Impact factor:   5.992


  3 in total

1.  Recombinant human growth hormone therapy in autosomal recessive polycystic kidney disease.

Authors:  Marusia Lilova; Bernard S Kaplan; Kevin E C Meyers
Journal:  Pediatr Nephrol       Date:  2002-11-26       Impact factor: 3.714

2.  Posterior reversible encephalopathy syndrome in a uremic patient with autosomal recessive polycystic kidney disease.

Authors:  Tadashi Yoshida; Ken Hiratsuka; Maho Yamashita; Ayumi Matsui; Matsuhiko Hayashi
Journal:  CEN Case Rep       Date:  2015-04-01

Review 3.  Looking at the (w)hole: magnet resonance imaging in polycystic kidney disease.

Authors:  Max Christoph Liebau; Andreas Lucas Serra
Journal:  Pediatr Nephrol       Date:  2012-12-14       Impact factor: 3.714

  3 in total

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