Related Experiment Video
Updated: Aug 10, 2026

Expression of Exogenous Cytokine in Patient-derived Xenografts via Injection with a Cytokine-transduced Stromal Cell Line
Published on: May 10, 2017
[X chromosome-linked lymphoproliferative syndrome (Duncan's disease)]
Insights
This study reports the first documented cases of X-linked lymphoproliferative syndrome (XLP) in Czechoslovakia, a fatal genetic disorder affecting two young brothers. The findings highlight a proliferative form of XLP presenting as severe infectious mononucleosis.
Area of Science:
- Immunology
- Genetics
- Pediatrics
Background:
- X-linked lymphoproliferative syndrome (XLP) is a rare primary immunodeficiency disorder.
- It primarily affects males and is characterized by an abnormal response to Epstein-Barr virus (EBV) infection.
- Previous literature lacks comprehensive descriptions of XLP cases in Czechoslovakia.
Abstract:
The authors describe two cases of fatal disease with the picture of acute haemoblastosis in male siblings aged 6 and 18 months. By combined retrospective evaluation of the two cases the authors reach the conclusion that it is the first case of an X chromosome-linked lymphoproliferative syndrome (XLP) described in Czechoslovakia. The authors discuss laboratory and clinical findings (dynamic of specific antibodies against EBV, histopathological finding, clinical evaluation, hypergammaglobulinaemia IgM, paraprotein IgM, genetic examination) and evaluate the disease as the proliferative form of XLP in the clinical variant of fatal infectious mononucleosis. The paper provides also some basic information on XLP, incl. some new findings.
More Related Videos
Related Concept Videos
Sex-linked Disorders
Sex Linked Disorders

