DELETION OF MITOCHONDRIAL-DNA IN PATIENT WITH CHRONIC TUBULOINTERSTITIAL NEPHRITIS

被引:48
作者
ROTIG, A
GOUTIERES, F
NIAUDET, P
RUSTIN, P
CHRETIEN, D
GUEST, G
MIKOL, J
GUBLER, MC
MUNNICH, A
机构
[1] HOP NECKER ENFANTS MALAD, INSERM, U393, UNITE RECH HANDICAPS GENET ENFANT, F-75743 PARIS 15, FRANCE
[2] HOP NECKER ENFANTS MALAD, INSERM, U192, UNITE RECH NEPHROL PEDIAT, F-75743 PARIS 15, FRANCE
[3] HOP NECKER ENFANTS MALAD, DEPT PEDIAT, F-75743 PARIS 15, FRANCE
[4] HOP LARIBOISIERE, SERV ANAT PATHOL, F-75475 PARIS, FRANCE
关键词
D O I
10.1016/S0022-3476(95)70359-4
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
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.
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页码:597 / 601
页数:5
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