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 st...

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Detalles Bibliográficos
Autores principales: Lim, Kenneth, Steele, David, Fenves, Andrew, Thadhani, Ravi, Heher, Eliot, Karaa, Amel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dustri-Verlag Dr. Karl Feistle 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5438005/
https://www.ncbi.nlm.nih.gov/pubmed/29043143
http://dx.doi.org/10.5414/CNCS109083

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5438005/
https://www.ncbi.nlm.nih.gov/pubmed/29043143
http://dx.doi.org/10.5414/CNCS109083

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