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- W2095482140 abstract "Mitochondrial cytopathies constitute a group of rare diseases that are characterized by their frequent multisystemic involvement, extreme variability of phenotype and complex genetics. In children, renal involvement is frequent and probably underestimated. The most frequent renal symptom is a tubular defect that, in most severe forms, corresponds to a complete De Toni-Debré-Fanconi syndrome. Incomplete proximal tubular defects and other tubular diseases have also been reported. In rare cases, patients present with chronic tubulo-interstitial nephritis or cystic renal diseases. Finally, a group of patients develop primarily a glomerular disease. These patients correspond to sporadic case reports or can be classified into two major defects, namely 3243 A>G tRNALEU mutations and coenzyme Q10 biosynthesis defects. The latter group is particularly important because it represents the only treatable renal mitochondrial defect. In this Educational Review, the principal characteristics of these diseases and the main diagnostic approaches are summarized." @default.
- W2095482140 created "2016-06-24" @default.
- W2095482140 creator A5054538151 @default.
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- W2095482140 date "2011-06-09" @default.
- W2095482140 modified "2023-10-01" @default.
- W2095482140 title "Renal involvement in mitochondrial cytopathies" @default.
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- W2095482140 doi "https://doi.org/10.1007/s00467-011-1926-6" @default.
- W2095482140 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3288375" @default.
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