Clinical and Complement Long-Term Follow-Up of a Pediatric Patient with C3 Mutation-Related Atypical Hemolytic Uremic Syndrome

We report a pediatric patient with atypical hemolytic uremic syndrome due to a C3 gain-of-function mutation diagnosed in infancy. She was treated from the start with a constant dose of 300 mg eculizumab every second week from the onset and followed by routine complement analyses for six years. Her c...

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Detalhes bibliográficos
Publicado no:Case Rep Nephrol
Main Authors: Bjerre, Anna, Bergseth, Grethe, Ludviksen, Judith Krey, Stokke, Arne, Bosnes, Vidar, Karpman, Diana, Mollnes, Tom Eirik
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi 2018
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6312603/
https://ncbi.nlm.nih.gov/pubmed/30662780
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2018/3810249
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