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
Autores principales: Trutin, Ivana, Oletić, Lea, Galešić Ljubanović, Danica, Turudić, Daniel, Milošević, Danko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sestre Milosrdnice University Hospital and Institute of Clinical Medical Research, Vinogradska cesta c. 29 Zagreb 2021
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8305348/
https://www.ncbi.nlm.nih.gov/pubmed/34588735
http://dx.doi.org/10.20471/acc.2021.60.01.21

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8305348/
https://www.ncbi.nlm.nih.gov/pubmed/34588735
http://dx.doi.org/10.20471/acc.2021.60.01.21

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