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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Dades bibliogràfiques
Publicat a:Clin Nephrol Case Stud
Autors principals: Lim, Kenneth, Steele, David, Fenves, Andrew, Thadhani, Ravi, Heher, Eliot, Karaa, Amel
Format: Artigo
Idioma:Inglês
Publicat: Dustri-Verlag Dr. Karl Feistle 2017
Matèries:
Case Report
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5438005/
https://ncbi.nlm.nih.gov/pubmed/29043143
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5414/CNCS109083
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