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X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia

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Description

XMEN is an X-linked recessive immunodeficiency characterized by CD4 (186940) lymphopenia, severe chronic viral infections, and defective T-lymphocyte activation (Li et al., 2011). Affected individuals have chronic EBV infection and are susceptible to the development of EBV-associated B-cell lymphoproliferative disorders. Magnesium supplementation may be therapeutic (summary by Li et al., 2014).

OMIM

  • Mode of Inheritance

  • X-linked recessive inheritance

VARIANTS

43

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Genes

External Links

  • OMIM

    300853

  • Orphanet

    317476

  • HPO
  • Medgen

    C3275445

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