| Autor: |
Micheletti MV; Pediatric Nephrology, Department of Pediatrics, University of Florence, Meyer Hospital, Florence, Italy., Lavoratti G, Gasperini S, Donati MA, Pela I |
| Jazyk: |
angličtina |
| Zdroj: |
Clinical nephrology [Clin Nephrol] 2011 Jul; Vol. 76 (1), pp. 68-73. |
| DOI: |
10.5414/cn106681 |
| Abstrakt: |
Hemolytic uremic syndrome (HUS) is characterized by microangiopathic hemolytic anemia, thrombocytopenia and acute renal failure. Besides diarrhea-associated HUS, due to verotoxin-producing Escherichia coli, in children HUS without prodromal diarrhea may be associated with other infectious and autoimmune diseases, genetic defects of the complement-regulator alternative-pathway, and inborn errors of vitamin B12 metabolism. Rhabdomyolysis is the dissolution of skeletal muscle due to various causes, including inborn errors of metabolism. Recurrent rhabdomyolysis and HUS have been previously described in one patient with a genetic defect of oxidative phosphorylation. We report the case of a 2-year-old boy with recurrent HUS and rhabdomyolysis in whom a succinate coenzyme Q reductase (complex II) deficiency was diagnosed. We hypothesize that defects of oxidative phosphorylation could be another etiological factor in atypical HUS. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
|
