Rötig A, Goutières F, Niaudet P, Rustin P, Chretien D, Guest G, Mikol J, Gubler M C, Munnich A
Unité de Recherches sur les Handicaps Génétiques de l'Enfant INSERM U393, Hôpital des Enfants-Malades, Paris, France.
J Pediatr. 1995 Apr;126(4):597-601. doi: 10.1016/s0022-3476(95)70359-4.
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.
我们报告了一名患有肾小管间质性肾炎的男孩存在线粒体DNA缺失(2.6 kb),该男孩随后发展为慢性肾衰竭和脑白质营养不良。血浆和脑脊液中乳酸值升高提示线粒体呼吸链存在缺陷。肌肉和脑白质中存在大量缺失的线粒体DNA。基于这一观察结果,我们建议在任何试图确定不明原因慢性肾小管间质性肾炎病因的尝试中,都要考虑氧化磷酸化的遗传缺陷,尤其是当涉及看似不相关的器官时。