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Neutrophil immunodeficiency syndrome

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Neutrophil immunodeficiency syndrome
Specialty Immunology
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]

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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.


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