Publication | Open Access
A Novel Mutation ApoE2 Kurashiki (R158P) in a Patient with Lipoprotein Glomerulopathy
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Citations
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References
2011
Year
GeneticsGenetic EpidemiologyPathologyHyperlipidemiaMetabolic SyndromeProteomicsChronic Kidney DiseaseAtherosclerosisLipid DisorderDyslipidemiaBiochemistryInherited Metabolic DiseaseLipoprotein GlomerulopathyVascular BiologySeveral ApolipoproteinAllelic VariantNatural SciencesLipoprotein MetabolismApoe2 PolymorphismMedicineNephrology
Lipoprotein glomerulopathy (LPG) is a rare glomerulopathy caused by lipoprotein thrombi. In almost all cases of LPG, several apolipoprotein (apo) E mutations were reported. Here, we present a case of LPG caused by a novel mutation that we named ApoE2 Kurashiki, which substitutes arginine with proline at apoE codon 158. ApoE2 polymorphism is well known for its relationship to type III hyperlipoproteinemia, and the common apoE2 isoform is encoded by the R158C allele. ApoE2 Kurashiki substitutes at the same codon and cannot be distinguished from common apoE2 by stan-dard apoE genotyping or phenotyping.
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