Focal segmental glomerulosclerosis with a mutation in the mitochondrially encoded NADH dehydrogenase 5 gene: A case report.
Mol Genet Metab Rep
; 35: 100963, 2023 Jun.
Article
em En
| MEDLINE
| ID: mdl-36941957
ATP, adenosine triphosphate; AiDIVs, age-inappropriately disarranged and irregularly sized vascular smooth muscle cells; COX IV, cytochrome c oxidase subunit 4; Case report; Cr, creatinine; FSGS, focal segmental glomerulosclerosis; Focal segmental glomerulosclerosis; GSECs, granular swollen epithelial cells; MELAS, mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes; MRC, mitochondrial respiratory chain; MT-ND5, mitochondrially encoded ND5; Mitochondrial nephropathy; NADH dehydrogenase 5; ND5, NADH dehydrogenase 5; OXPHOS:, oxidative phosphorylation; Podocyte; ReCPos, red-coloured podocytes; eGFR, estimated glomerular filtration rate; mtDNA, mitochondrial DNA; nDNA, nuclear DNA; sCr, serum creatinine
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Idioma:
En
Revista:
Mol Genet Metab Rep
Ano de publicação:
2023
Tipo de documento:
Article
País de afiliação:
Japão