Common variable immunodeficiency and hemophagocytic features associated with a FAS gene mutation

J Allergy Clin Immunol. 2011 Jun;127(6):1411-4.e2. doi: 10.1016/j.jaci.2011.01.046. Epub 2011 Mar 29.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Autoimmune Lymphoproliferative Syndrome / complications*
  • Autoimmune Lymphoproliferative Syndrome / genetics*
  • Autoimmune Lymphoproliferative Syndrome / immunology
  • B-Lymphocytes / immunology
  • Child, Preschool
  • Common Variable Immunodeficiency / complications*
  • Common Variable Immunodeficiency / genetics*
  • Common Variable Immunodeficiency / immunology
  • Female
  • Humans
  • Lymphohistiocytosis, Hemophagocytic / complications*
  • Lymphohistiocytosis, Hemophagocytic / genetics*
  • Lymphohistiocytosis, Hemophagocytic / immunology
  • Male
  • Mutation
  • Pedigree
  • T-Lymphocytes / immunology
  • fas Receptor / genetics*

Substances

  • FAS protein, human
  • fas Receptor