X-linked immunodeficiencies

Curr Opin Genet Dev. 1994 Jun;4(3):401-6. doi: 10.1016/0959-437x(94)90028-0.

Abstract

In the past year, researchers have identified the genes responsible for X-linked severe combined immunodeficiency (encoding a cytokine receptor protein), X-linked agammaglobulinemia (encoding a cytoplasmic tyrosine kinase) and X-linked hyper IgM syndrome (encoding the ligand for CD40). Although these three genes are completely unrelated, it is of interest that all are lineage-specific genes that are involved in the control of lymphocyte proliferation or differentiation.

Publication types

  • Review

MeSH terms

  • Agammaglobulinemia / genetics
  • Child
  • Female
  • Genetic Linkage
  • Humans
  • Hypergammaglobulinemia / genetics
  • Immunoglobulin M
  • Immunologic Deficiency Syndromes / genetics*
  • Infant, Newborn
  • Male
  • Severe Combined Immunodeficiency / genetics
  • X Chromosome*

Substances

  • Immunoglobulin M