Focal segmental glomerulosclerosis associated with mitochondrial cytopathy

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Focal segmental glomerulosclerosis associated with mitochondrial disease

Primary mitochondrial diseases (MD) are complex, heterogeneous inherited diseases caused by mutations in either the mitochondrial or nuclear DNA. Glomerular diseases in MD have been reported with tRNA mutation m.3243A>G causing a syndrome of mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS). We describe here a case of focal segmental glomerulosclerosis (FSGS) ass...

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ژورنال

عنوان ژورنال: Kidney International

سال: 2000

ISSN: 0085-2538,1523-1755

DOI: 10.1046/j.1523-1755.2000.00356.x