Literature DB >> 7699541

Deletion of mitochondrial DNA in patient with chronic tubulointerstitial nephritis.

A Rötig1, F Goutières, P Niaudet, P Rustin, D Chretien, G Guest, J Mikol, M C Gubler, A Munnich.   

Abstract

We report a mitochondrial DNA deletion (2.6 kb) in a boy with tubulointerstitial nephritis in whom chronic renal failure and leukodystrophy subsequently developed. Elevated lactate values in plasma and cerebrospinal fluid were suggestive of a defect in the mitochondrial respiratory chain. High amounts of deleted mitochondrial DNA were present in muscle and cerebral white matter. On the basis of this observation, we suggest giving consideration to genetic defects of oxidative phosphorylation in any attempt to determine the origin of unexplained chronic tubulointerstitial nephritis, especially when seemingly unrelated organs are involved.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 7699541     DOI: 10.1016/s0022-3476(95)70359-4

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  17 in total

Review 1.  Mitochondrial Diseases Part I: mouse models of OXPHOS deficiencies caused by defects in respiratory complex subunits or assembly factors.

Authors:  Alessandra Torraco; Susana Peralta; Luisa Iommarini; Francisca Diaz
Journal:  Mitochondrion       Date:  2015-02-04       Impact factor: 4.160

Review 2.  Mitochondrial disorders and the kidney.

Authors:  P Niaudet
Journal:  Arch Dis Child       Date:  1998-04       Impact factor: 3.791

Review 3.  Clinical presentation of mitochondrial disorders in childhood.

Authors:  A Munnich; A Rötig; D Chretien; V Cormier; T Bourgeron; J P Bonnefont; J M Saudubray; P Rustin
Journal:  J Inherit Metab Dis       Date:  1996       Impact factor: 4.982

Review 4.  Mitochondria in Acute Kidney Injury.

Authors:  Kenneth M Ralto; Samir M Parikh
Journal:  Semin Nephrol       Date:  2016-01       Impact factor: 5.299

5.  Mitochondrial DNA deletion in a girl with Fanconi's syndrome.

Authors:  Kam Ming Au; Shing Chi Lau; Yuen Fun Mak; Wai Ming Lai; Tat Chong Chow; Mo Lung Chen; Man Chun Chiu; Albert Yan Wo Chan
Journal:  Pediatr Nephrol       Date:  2006-09-12       Impact factor: 3.714

Review 6.  Renal transplant in methylmalonic acidemia: could it be the best option? Report on a case at 10 years and review of the literature.

Authors:  Riccardo Lubrano; Marco Elli; Massimo Rossi; Elisabetta Travasso; Claudia Raggi; Paola Barsotti; Claudia Carducci; Pasquale Berloco
Journal:  Pediatr Nephrol       Date:  2007-03-31       Impact factor: 3.714

7.  Respiratory chain deficiency presenting as congenital nephrotic syndrome.

Authors:  Alice Goldenberg; Linh Huynh Ngoc; Marie-Christine Thouret; Valérie Cormier-Daire; Marie-France Gagnadoux; Dominique Chrétien; Catherine Lefrançois; Vanna Geromel; Agnès Rötig; Pierre Rustin; Arnold Munnich; Véronique Paquis; Corinne Antignac; Marie-Claire Gubler; Patrick Niaudet; Pascale de Lonlay; Etienne Bérard
Journal:  Pediatr Nephrol       Date:  2005-01-29       Impact factor: 3.714

8.  Renal pathology in children with mitochondrial diseases.

Authors:  Elena Martín-Hernández; M Teresa García-Silva; Julia Vara; Yolanda Campos; Ana Cabello; Rafael Muley; Pilar Del Hoyo; Miguel Angel Martín; Joaquín Arenas
Journal:  Pediatr Nephrol       Date:  2005-06-24       Impact factor: 3.714

9.  Nephropathy and growth hormone deficiency in a patient with mitochondrial tRNA(Leu(UUR)) mutation.

Authors:  T Yorifuji; M Kawai; T Momoi; H Sasaki; K Furusho; J Muroi; K Shimizu; Y Takahashi; M Matsumura; M Nambu; T Okuno
Journal:  J Med Genet       Date:  1996-07       Impact factor: 6.318

10.  An autopsy case of chronic progressive external ophthalmoplegia with renal insufficiency.

Authors:  Takashi Yuri; Yaeko Kondo; Keiko Kohno; Yen-Chang Lei; Seika Kanematsu; Maki Kuwata; Toshiji Iwasaka; Airo Tsubura
Journal:  Med Mol Morphol       Date:  2008-12-24       Impact factor: 2.309

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.