Wiskott-Aldrich syndrome; an x-linked primary immunodeficiency disease with unique and characteristic features

Allergol Int. 2012 Jun;61(2):183-9. doi: 10.2332/allergolint.11-RAI-0412. Epub 2012 Feb 25.

Abstract

Wiskott-Aldrich syndrome (WAS) is an X-linked primary immunodeficiency disease with unique and characteristic features. In 1994, the responsible gene for WAS, the WASP gene on X-chromosome, was identified. Since then, renewed clinical and basic researches of WAS have started and remarkably developed. I will comment on recent progress in the clinical and basic researches of WAS, including some topics reported by our and other groups.

Publication types

  • Review

MeSH terms

  • Animals
  • Eczema / immunology
  • Genes, X-Linked / genetics
  • Genes, X-Linked / immunology
  • Genetic Therapy
  • Hematopoietic Stem Cell Transplantation
  • Hemorrhage / immunology
  • Humans
  • Immunity / genetics
  • Infant, Newborn
  • Male
  • Mutation / genetics
  • Thrombocytopenia / immunology
  • Wiskott-Aldrich Syndrome / diagnosis*
  • Wiskott-Aldrich Syndrome / genetics*
  • Wiskott-Aldrich Syndrome / immunology
  • Wiskott-Aldrich Syndrome Protein / genetics
  • Wiskott-Aldrich Syndrome Protein / metabolism*

Substances

  • Wiskott-Aldrich Syndrome Protein