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Glomerulopathy with Homozygous Apolipoprotein E2: A Report of Three Cases and Review of the Literature

Most cases of type III hyperlipoproteinemia are accounted for by apolipoprotein E2 (apoE2) homozygotes, a genetic mutation of apoE (Arg158Cys). Glomerulopathy with homozygous apoE2 is rare and characterized by marked foam cell infiltration in the glomerular capillaries and mesangium. Here, we report...

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Detalles Bibliográficos
Autores principales:	Kawanishi, Kunio, Sawada, Anri, Ochi, Ayami, Moriyama, Takahito, Mitobe, Michihiro, Mochizuki, Toshio, Honda, Kazuho, Oda, Hideaki, Nishikawa, Toshio, Nitta, Kosaku
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	S. Karger AG 2013
Materias:	Published online: November, 2013
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3924710/ https://www.ncbi.nlm.nih.gov/pubmed/24570682 http://dx.doi.org/10.1159/000356849

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