Rare form of mitochondriopathy with the deficiency of coenzyme Q: Steroid-resistant nephrotic syndrome with CoQ6 mutation
Abstract
We present an observation of early-onset steroid-resistant nephrotic syndrome with sensorineural deafness as a consequence of CoQ10 deficiency, with ultrastructural renal lesion characterized by widespread proliferation of abnormal mitochondria in glomerular cells.
About the Authors
T. V. Vashurina
НИИ педиатрии ФГБУ «НЦЗД» РАМН
Russian Federation
Russian Federation
O. I. Zrobok
НИИ педиатрии ФГБУ «НЦЗД» РАМН
Russian Federation
Russian Federation
T. V. Margieva
НИИ педиатрии ФГБУ «НЦЗД» РАМН
Russian Federation
Russian Federation
M. V. Matveeva
НИИ педиатрии ФГБУ «НЦЗД» РАМН
Russian Federation
Russian Federation
N. V. Andreenko
НИИ педиатрии ФГБУ «НЦЗД» РАМН
Russian Federation
Russian Federation
L. V. Leonova
НИИ педиатрии ФГБУ «НЦЗД» РАМН
Russian Federation
Russian Federation
P. E. Povilaitite
ГУЗ Патологоанатомическое бюро Ростовской области
Russian Federation
Russian Federation
A. N. Tsygin
НИИ педиатрии ФГБУ «НЦЗД» РАМН
Russian Federation
Russian Federation
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Review
For citations:
Vashurina T.V., Zrobok O.I., Margieva T.V., Matveeva M.V., Andreenko N.V., Leonova L.V., Povilaitite P.E., Tsygin A.N. Rare form of mitochondriopathy with the deficiency of coenzyme Q: Steroid-resistant nephrotic syndrome with CoQ6 mutation. Nephrology and Dialysis. 2012;14(2):133-136. (In Russ.)
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