WHIM syndrome

Mayo Clinic Proceedings

Volumn 82, Issue 9, 2007, Pages 1031-

  Hagan, John B ^a   Nguyen, Phuong L ^a  

^a MAYO CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANTINUCLEAR ANTIBODY; GRANULOCYTE ANTIBODY; IMMUNOGLOBULIN A; IMMUNOGLOBULIN G; IMMUNOGLOBULIN G3; IMMUNOGLOBULIN M;

ADULT; ANTIBODY RESPONSE; ARTICLE; BONE MARROW BIOPSY; CASE REPORT; DIPHTHERIA; DNA SEQUENCE; HUMAN; HUMAN IMMUNODEFICIENCY VIRUS; IMMUNOGLOBULIN DEFICIENCY; INFECTION; INFLUENZA VIRUS B; MALE; MICROSCOPY; NEUTROPENIA; NEUTROPHIL COUNT; OTITIS MEDIA; SKIN ABSCESS; VERRUCA VULGARIS; WHIM SYNDROME;

EID: 34548411688     PISSN: 00256196     EISSN: None     Source Type: Journal    
DOI: 10.4065/82.9.1031     Document Type: Article

References (5)

1. Gorlin RJ, Gelb B, Diaz GA, Lofsness KG, Pittelkow MR, Fenyk JR. WHIM syndrome, an autosomal dominant disorder: clinical, hematological, and molecular studies. Am J Med Genet. 2000;91:368-376.
2. Diaz GA. CXCR4 mutations in WHIM syndrome: a misguided immune system? Immunol Rev. 2005;203:235-243.
3. Krill CE, Smith HD, Mauer AM. Chronic idiopathic granulocytopenia. N Engl J Med. 1964;270:973-979.
4. Zuelzer WW. "Myelokathexis" - a new form of chronic granulocytopenia: report of a case. N Engl J Med. 1964;270:699-704.
5. Hernandez PA, Gorlin RJ, Lukens JN, et al. Mutations in the chemokine receptor gene CXCR4 are associated with WHIM syndrome, a combined immunodeficiency disease. Nat Genet. 2003;34:70-74.