Case Report: Membranoproliferative Glomerulonephritis, a Rare Clinical Manifestation of Abernethy Malformation Type II

This report describes an 8-year-old male who presented with clinical manifestations including systemic edema, heavy proteinuria, hypoproteinemia, and persistent hypocomplementemia. Arachnoid cysts and focal nodular hyperplasia were also detected. Imaging examination and renal biopsy were performed,...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Front Pediatr
Päätekijät: He, Xue, Zhu, Yueling, Fu, Haidong, Feng, Chunyue, Liu, Zhixia, Gu, Weizhong, Jin, Yanyan, Yang, Binbin, Shen, Huijun
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Frontiers Media S.A. 2021
Aiheet:
Pediatrics
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC8010253/
https://ncbi.nlm.nih.gov/pubmed/33816407
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fped.2021.647364
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