Mitochondrial DNA deletion in a girl with Fanconi’s syndrome-Reference-Cited by-同舟云学术

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Mitochondrial DNA deletion in a girl with Fanconi’s syndrome

Published:2007-01 Issue:1 Volume:22 Page:136-140
ISSN:0931-041X
Container-title:Pediatric Nephrology
language:en
Short-container-title:Pediatr Nephrol

Author:

Au Kam Ming,Lau Shing Chi,Mak Yuen Fun,Lai Wai Ming,Chow Tat Chong,Chen Mo Lung,Chiu Man Chun,Chan Albert Yan Wo

Publisher

Springer Science and Business Media LLC

Subject

Nephrology,Pediatrics, Perinatology, and Child Health

Link

http://link.springer.com/content/pdf/10.1007/s00467-006-0288-y.pdf

Reference16 articles.

1. Moraes CT, DiMauro S, Zeviani M, Lombes A, Shakske S, Miranda AF, Nakase H, Bonilla E, Werneck LC, Servidei S, Nonaka I, Koga Y, Spiro AJ, Brownell KW, Schmidt B, Schotland DL, Zupanc M, DeVivo DC, Schon EA, Rowland LP (1989) Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns–Sayre syndrome. N Engl J Med 320:1293–1299

2. Wong LJC (2001) Recognition of mitochondrial DNA deletion syndrome with non-neuromuscular multisystemic manifestation. Genet Med 3:399–404

3. Eviatar L, Shanske S, Gauthier B, Abrams C, Maytal J, Slavin M, Valderrama E, DiMauro S (1990) Kearns–Sayre syndrome presenting as renal tubular acidosis. Neurology 40:1761–1763

4. Grünfeld JP, Niaudet P, Rötig A (1996) Renal involvement in mitochondrial cytopathies. Nephrol Dial Transplant 11:760–761

5. Niaudet P, Heidet L, Munnich A, Schmitz J, Bouissou F, Gubler MC, Rötig A (1994) Deletion of the mitochondrial DNA in a case of de Toni–Debré–Fanconi syndrome and Pearson syndrome. Pediatr Nephrol 8:164–168

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