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Article

[X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia: report of a family and literature review].

Zhonghua er ke za zhi = Chinese journal of pediatrics - 2 Jan 2018

He T Y, Xia Y, Li C G, Li C R, Qi Z X, Yang J

Abstract excerpt

Objective: To investigate the clinical features and genetic characteristics of cases with X-linked immunodeficiency with magnesium defect, Epstein-Barr virus (EBV) infection, and neoplasia (XMEN). Methods: Characteristics of clinical material, immunological data and gene mutation of two cases with XMEN in the same family in China were retrospectively analyzed. The related reports literature were searched by using...

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Identifiers

PMID: 29342998
DOI: 10.3760/cma.j.issn.0578-1310.2018.01.013

Genes

MAGT1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

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[X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia: report of a family and literature review].PMID 29342998Read ↗

X-linked immunodeficiency with magnesium defect, Epstein–Barr virus infection, and neoplasia diseaseSemantic proximity Read ↗

Scales of Magt1 Gene: Novel Mutations, Different Presentations.Semantic proximity Read ↗

[XMEN disease diagnosed following persistent Epstein-Barr virus viremia and recurrent lymphadenopathy].Semantic proximity Read ↗

XMEN-associated Systemic EBV-positive T-cell Lymphoma of Childhood: Report of Two Cases and Literature Review.Semantic proximity Read ↗

An Update on XMEN Disease.Semantic proximity Read ↗

Lymphoma arising in the setting of inborn errors of immunity: A six-case series of XMEN-associated pediatric lymphomaSemantic proximity Read ↗

Defective glycosylation and multisystem abnormalities characterize the primary immunodeficiency XMEN diseaseSemantic proximity Read ↗

MAGT1 gene mutation causes myositis and CD127 expression downregulationSemantic proximity Read ↗

Identification of a novel MAGT1 mutation supports a diagnosis of XMEN disease.Semantic proximity Read ↗

Identification of a novel mutation in MAGT1 and progressive multifocal leucoencephalopathy in a 58-year-old man with XMEN disease.Semantic proximity Read ↗

Case Report: A successful case of allogeneic stem cell transplantation for pediatric XMEN characterized by neutropenia.Semantic proximity Read ↗

Modifier-Sensitive Phenotypic Divergence in XMEN Disease (MAGT1 Deficiency): Neurodegenerative and Hematologic TrajectoriesSemantic proximity Read ↗

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