Neutrophil immunodeficiency syndrome

Neutrophil immunodeficiency syndrome
SpecialtyImmunology
Frequency<1 / 1 000 000[1]

Neutrophil immunodeficiency syndrome is a condition caused by mutations in the Rac2 gene.[2] It is a primary immunodeficiency by neutrophilia with severe neutrophil dysfunction, leukocytosis, a predisposition to bacterial infections and poor wound healing, including an absence of pus in infected areas. There have been 2 reported cases as of March 2010.[3]

See also

References

  1. ^ RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Neutrophil immunodeficiency syndrome". www.orpha.net. Retrieved 18 March 2019.{{cite web}}: CS1 maint: numeric names: authors list (link)
  2. ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 978-1-4160-2999-1.
  3. ^ "Orphanet: Infantile LAD-like disease due to RAC2 deficiency". www.orpha.net. Retrieved 2026-02-13.


This article is issued from Wikipedia. The text is available under Creative Commons Attribution-Share Alike 4.0 unless otherwise noted. Additional terms may apply for the media files.