Nijmegen syndrome in childhood: a clinical case

Nijmegen syndrome is a rare monogenic pathology with an autosomal recessive type of inheritance. The disease is manifested by congenital developmental anomalies and microcephaly, primary immunodeficiency, frequent recurrent viral and bacterial infections, retardation in physical and neuropsychic dev...

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Bibliographic Details
Main Authors: N. V. Malyuzhinskaya, M. A. Morgunova, I. V. Petrova, O. V. Polyakova, V. V. Samokhvalova, A. V. Bayurov, G. V. Klitochenko
Format: Article
Language:Russian
Published: ABV-press 2024-04-01
Series:Онкогематология
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Online Access:https://oncohematology.abvpress.ru/ongm/article/view/919
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