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A rare cause of childhood-onset nephrotic syndrome: lipoprotein glomerulopathy.

Clinical nephrology - 1 Sept 2012

Liao Min-Tser, Tsai I-Jung, Cheng Hui-Teng, Lin Wei-Chou, Chang Yen-Wen, Lin Yi-Heng, Tsau Yong-Kwei

Abstract excerpt

We report on a 12-year-old female patient with lipoprotein glomerulopathy (LPG) who was proven to be heterozygous for ApoE2 Kyoto (Arg25Cys). Her family members have the same variant but do not have obvious signs of renal function impairment. Six months of treatment with a statin caused significa...

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PMID: 22874113
DOI: 10.5414/cn106876

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Prepared record publication-22874113-2026-09-05.1. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 5 Sept 2026.

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