関連する実験動画

Updated: Sep 9, 2025

Analyses of Proteinuria, Renal Infiltration of Leukocytes, and Renal Deposition of Proteins in Lupus-prone MRL/lpr Mice
09:43

Analyses of Proteinuria, Renal Infiltration of Leukocytes, and Renal Deposition of Proteins in Lupus-prone MRL/lpr Mice

Published on: June 8, 2022

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ダブルグロメルーラ病理の希少な症例:アルポート症候群と免疫複合体媒介のMPGN

Seyda Gul Ozcan1, Eylul Koc2, Ahmet Murt3

  • 1Cerrahpasa Medical Faculty, Division of Nephrology, Istanbul University-Cerrahpasa, Istanbul, Turkey. seydagulozcan@gmail.com.

BMC nephrology
|September 3, 2025
PubMed
まとめ

免疫複合体媒介性膜増殖性グルメロネフリス (IC-MPGN) とアルポート症候群の並存はまれに観察された. 早期の腎臓生検と遺伝子検査は 複雑な球疾患の管理に不可欠です

キーワード:
アルポート症候群遺伝的な腎臓病免疫複合体媒介のMPGN

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