A Child with Dense Deposit Disease and Decreased Classic Complement Pathway Activity

A Child with Dense Deposit Disease and Decreased Classic Complement Pathway Activity

We report a rare case of nephritic syndrome underlying dense deposit disease (DDD) with alternative complement pathway dysfunction explained with both C3 nephritic factor (C3NeF) antibodies and DDD associated polymorphism of factor H. An 8-year-old boy presented with macroscopic hematuria, hypert...

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Bibliographic Details
Main Authors: Ivana Trutin, Lea Oletić, Danica Galešić Ljubanović, Daniel Turudić, Danko Milošević
Format: Article
Language:English
Published: Sestre Milosrdnice University hospital, Institute of Clinical Medical Research 2021-01-01
Series:Acta Clinica Croatica
Subjects:
Dense deposit disease
C3 glomerulopathy
Children
Nephritic syndrome
Online Access:https://hrcak.srce.hr/file/378136

Internet

https://hrcak.srce.hr/file/378136

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