Nephrology Dialysis Transplantation · 2010 · 25 citations · 10 references
MedicineGeneticsNephrologyHuman GeneticsMedical GeneticsRenal PathophysiologyGenetic DisordersGlomerular DiseasesGlomerular PathophysiologyHereditary Kidney DiseasesHereditary Renal DiseasesRenal DiseaseApoe GeneticsApolipoprotein DisordersApolipoprotein E VariantsGenetic Glomerular DisordersGlomerular Capillary DamageGlomerular Capillary InjuryMutation
Lipoprotein glomerulopathy is a rare disease diagnosed by unique histopathologic findings of glomerular capillary dilatation by lipoprotein thrombi. The disease is caused by mutations in apoE, the gene that encodes apolipoprotein E. To date, <80 cases have been reported in the medical literature, nearly all of which are from Japan or China. Only five cases from the United States have previously been reported, of which three patients were of European ancestry. Here, we present the fourth case of lipoprotein glomerulopathy in a European-American man. Whereas prior European-American patients with lipoprotein glomerulopathy were found to have the previously reported apoE Kyoto genotype, the patient presented here was found to have a novel mutation that we have named apoE Las Vegas.
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Apolipoprotein E Sendai (arginine 145-->proline)
Shin Oikawa, Akihiro Matsunaga, Takao Saito et al. · Journal of the American Society of Nephrology · 1997 · 104 citations
A novel apolipoprotein E mutation, E2 (Arg25Cys), in lipoprotein glomerulopathy
Akira Matsunaga, Junichi Sasaki, Takeo Komatsu et al. · Kidney International · 1999 · 94 citations · Full text
Medicine, Genetics, Nephrology +14