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, hypertens...

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Detalles Bibliográficos
Publicado en:Acta Clin Croat
Main Authors: Trutin, Ivana, Oletić, Lea, Galešić Ljubanović, Danica, Turudić, Daniel, Milošević, Danko
Formato: Artigo
Idioma:Inglês
Publicado: Sestre Milosrdnice University Hospital and Institute of Clinical Medical Research, Vinogradska cesta c. 29 Zagreb 2021
Assuntos:
Case Reports
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC8305348/
https://ncbi.nlm.nih.gov/pubmed/34588735
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.20471/acc.2021.60.01.21
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