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Article

Novel Mutations in SH2D1A Gene in X-linked Lymphoproliferative Syndrome, Diagnosed After B-Cell Non-Hodgkin Lymphoma.

Journal of pediatric hematology/oncology - 1 May 2017

Sharapova Svetlana O, Fedorova Alina S, Pashchenko Olga E, Vahliarskaya Svetlana S, Guryanova Irina E, Migas Alexandr A, Kondratenko Irina V, Aleinikova Olga V

Abstract excerpt

BACKGROUND: X-linked lymphoproliferative disease type I (XLP I) is caused by mutations in the SH2D1A gene and characterized mainly by hypogammaglobulinemia and abnormal response to Epstein-Barr virus with a high predisposition to B-cell non-Hodgkin lymphoma development. OBSERVATIONS: In this article, we describe the experience of 2 centers in Belarus and in Russia that follow 3 male patients who were diagnosed...

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PMID: 28267077
DOI: 10.1097/MPH.0000000000000815

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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