Literature DB >> 11325702

Adenine phosphoribosyltransferase deficiency and renal allograft dysfunction.

B Benedetto1, R Madden, A Kurbanov, G Braden, J Freeman, G S Lipkowitz.   

Abstract

Adenine phosphoribosyltransferase (APRT) deficiency is a rarely diagnosed cause of renal allograft dysfunction. We report the case of a 42-year-old man who presented in 1996 with idiopathic renal failure. Native kidney biopsy showed extensive microcrystalline interstitial nephritis. The patient subsequently underwent a living-related kidney transplant with excellent early graft function. During the next year, however, he had worsening allograft function, and allograft biopsy showed recurrent interstitial nephritis. Further chemical and spectroscopic analysis showed this lesion to be an annular microcrystalline nephritis consistent with APRT deficiency. This diagnosis was confirmed on erythrocyte assay. Treatment with allopurinol and a low-purine diet led to improvement and stabilization of renal function. APRT is a rare cause of renal allograft dysfunction requiring a high index of suspicion for early diagnosis and treatment. Increased physician awareness in the United States may hasten diagnosis and limit the morbidity associated with this disease.

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Year:  2001        PMID: 11325702     DOI: 10.1016/s0272-6386(05)90001-2

Source DB:  PubMed          Journal:  Am J Kidney Dis        ISSN: 0272-6386            Impact factor:   8.860


  16 in total

1.  A rare case of primary non-function of renal allograft due to adenine phosphoribosyltransferase deficiency.

Authors:  Benoit Brilland; Jean-François Augusto; Anne Croue; Jean-François Subra; Johnny Sayegh
Journal:  Int Urol Nephrol       Date:  2015-08-09       Impact factor: 2.370

2.  Adenine phosphoribosyltransferase deficiency as a rare cause of renal allograft dysfunction.

Authors:  Kati Kaartinen; Ulla Hemmilä; Kaija Salmela; Anne Räisänen-Sokolowski; Timo Kouri; Satu Mäkelä
Journal:  J Am Soc Nephrol       Date:  2014-01-23       Impact factor: 10.121

3.  Adenine phosphoribosyltransferase deficiency: an underdiagnosed cause of lithiasis and renal failure.

Authors:  Giuseppina Marra; Paolo Gilles Vercelloni; Alberto Edefonti; Gianantonio Manzoni; Maria Angela Pavesi; Giovanni Battista Fogazzi; Giuseppe Garigali; Lionel Mockel; Irene Ceballos Picot
Journal:  JIMD Rep       Date:  2011-12-21

4.  Phenotype and genotype characterization of adenine phosphoribosyltransferase deficiency.

Authors:  Guillaume Bollée; Cécile Dollinger; Lucile Boutaud; Delphine Guillemot; Albert Bensman; Jérôme Harambat; Patrice Deteix; Michel Daudon; Bertrand Knebelmann; Irène Ceballos-Picot
Journal:  J Am Soc Nephrol       Date:  2010-02-11       Impact factor: 10.121

5.  Crystalline Nephropathy due to APRT Deficiency: A Preventable Cause of Renal and Renal Allograft Failure.

Authors:  Prashant Rajput; Zaheer A Virani; Bharat V Shah
Journal:  Indian J Nephrol       Date:  2020-04-01

6.  APRT deficiency: the need for early diagnosis.

Authors:  Aamira Huq; Kushma Nand; Rajiv Juneja; Ingrid Winship
Journal:  BMJ Case Rep       Date:  2018-10-23

Review 7.  Hereditary causes of kidney stones and chronic kidney disease.

Authors:  Vidar O Edvardsson; David S Goldfarb; John C Lieske; Lada Beara-Lasic; Franca Anglani; Dawn S Milliner; Runolfur Palsson
Journal:  Pediatr Nephrol       Date:  2013-01-20       Impact factor: 3.714

8.  Recurrent 2,8-dihydroxyadenine nephropathy: a rare but preventable cause of renal allograft failure.

Authors:  M Zaidan; R Palsson; E Merieau; E Cornec-Le Gall; A Garstka; U Maggiore; P Deteix; M Battista; E-R Gagné; I Ceballos-Picot; J-P Duong Van Huyen; C Legendre; M Daudon; V O Edvardsson; B Knebelmann
Journal:  Am J Transplant       Date:  2014-10-10       Impact factor: 8.086

9.  Kidney Transplant Outcomes in Patients With Adenine Phosphoribosyltransferase Deficiency.

Authors:  Hrafnhildur Linnet Runolfsdottir; Runolfur Palsson; Inger M Sch Agustsdottir; Olafur S Indridason; Jennifer Li; Myriam Dao; Bertrand Knebelmann; Dawn S Milliner; Vidar O Edvardsson
Journal:  Transplantation       Date:  2020-10       Impact factor: 5.385

10.  Ultra-rare renal diseases diagnosed with whole-exome sequencing: Utility in diagnosis and management.

Authors:  Jiwon Jung; Joo Hoon Lee; Young Seo Park; Go Hun Seo; Changwon Keum; Hee Gyung Kang; Hajeong Lee; Sang Koo Lee; Sang Taek Lee; Heeyeon Cho; Beom Hee Lee
Journal:  BMC Med Genomics       Date:  2021-07-03       Impact factor: 3.063

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