The Rationale of Complement Blockade of the MCP(ggaac) Haplotype following Atypical Hemolytic Uremic Syndrome of Three Southeastern European Countries with a Literature Review

We present eight cases of the homozygous MCPggaac haplotype, which is considered to increase the likelihood and severity of atypical hemolytic uremic syndrome (aHUS), especially in combination with additional risk aHUS mutations. Complement blockade (CBT) was applied at a median age of 92 months (IQ...

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Detalles Bibliográficos
Autores principales: Turudic, Daniel, Pokrajac, Danka, Tasic, Velibor, Kasumovic, Dino, Prohaszka, Zoltan, Milosevic, Danko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Brief Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10487996/
https://www.ncbi.nlm.nih.gov/pubmed/37685848
http://dx.doi.org/10.3390/ijms241713041

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10487996/
https://www.ncbi.nlm.nih.gov/pubmed/37685848
http://dx.doi.org/10.3390/ijms241713041

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