Hypogammaglobulinemia in a child with atypical hemolytic-uremic syndrome

Hypogammaglobulinemia in a child with atypical hemolytic-uremic syndrome

We present a unique clinical case of an atypical hemolytic-uremic syndrome in a child. The mutation in exon 6 of the CD46 gene (chr1:207940532G>C) leads to a homozygous or hemizygous missense substitution. An 8-year-old girl was urgently hospitalized with symptoms of hemorrhagic syndrome and...

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Bibliographic Details
Main Authors: N. S. Zhuravleva, V. I. Kutuzova, M. R. Almerzaeva, N. Yu. Mineeva, O. Yu. Maslov
Format: Article
Language:Russian
Published: St. Petersburg branch of the Russian Association of Allergologists and Clinical Immunologists 2024-09-01
Series:Медицинская иммунология
Subjects:
children
thrombotic microangiopathy
hypogammaglobulinemia
cd46 gene mutation
complement-blocking therapy
Online Access:https://www.mimmun.ru/mimmun/article/view/3094
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