X-linked lymphoproliferative syndrome

  • Y. Romanyshyn -
  • L. Kostyuchenko -
  • L. Vygovska Львівська обласна дитяча спеціалізована клінічна лікарня
Keywords: X-linked lymphoproliférative syndrome, Duncan syndrome, EBV, SLAM-associated protein, XIAP, hemopoetic stem cell transplantation

Abstract

X-linked lymphoproliférative syndrome (Duncan syndrome) is a rare genetically primary imm­unodeficiency, typically characterized by occurrence of fatal EBV-induced mononucleosis and severe changes in immunologic studies. This article contains reference list and clinical case of the patient with XLP, who presented typical clinical picture and changes in immunologic studies. Mutation of SAP-gene did not revealed.

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Published
2020-03-11
How to Cite
Romanyshyn, Y., Kostyuchenko, L., & Vygovska, L. (2020). X-linked lymphoproliferative syndrome. Farmatsevtychnyi Zhurnal, (1), 101-107. Retrieved from https://pharmj.org.ua/index.php/journal/article/view/877
Section
Original Articles