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,...

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Detalles Bibliográficos
Autores principales: He, Xue, Zhu, Yueling, Fu, Haidong, Feng, Chunyue, Liu, Zhixia, Gu, Weizhong, Jin, Yanyan, Yang, Binbin, Shen, Huijun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8010253/
https://www.ncbi.nlm.nih.gov/pubmed/33816407
http://dx.doi.org/10.3389/fped.2021.647364

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8010253/
https://www.ncbi.nlm.nih.gov/pubmed/33816407
http://dx.doi.org/10.3389/fped.2021.647364

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