Association of humoral immunodeficiency, cleidocranial dysplasia, and von Willebrand's disease in a family cluster [1]

Journal of Allergy and Clinical Immunology

Volumn 107, Issue 4, 2001, Pages 742-

  Kelkar, Pramod S ^a   Ten, Rosa M ^a  

^a MAYO CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ANTIBODY RESPONSE; CASE REPORT; CLEIDOCRANIAL DYSPLASIA; DISEASE ASSOCIATION; FAMILIAL DISEASE; FEMALE; GENETIC DISORDER; HUMAN; HUMORAL IMMUNE DEFICIENCY; LETTER; OPPORTUNISTIC INFECTION; PEDIGREE; PRIORITY JOURNAL; T LYMPHOCYTE; VON WILLEBRAND DISEASE; WISKOTT ALDRICH SYNDROME;

EID: 0035041065     PISSN: 00916749     EISSN: None     Source Type: Journal    
DOI: 10.1067/mai.2001.112133     Document Type: Letter

References (4)

1. Dandy-Walker (like) malformation, atrio-ventricular septal defect and a similar pattern of minor anomalies in 2 sisters: A new syndrome?
2. Immunodeficiency in a patient with Baller-Gerold syndrome: A reason for early demise?
3. An immunodeficiency characterized by impaired antibody responses to polysaccharides
4. Selective defect in the antibody response to H. influenzae type b in children with recurrent infectious and normal serum IgG subclass levels