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Clinical and Diagnostic Laboratory Immunology, November 2004, p. 1192-1193, Vol. 11, No. 6
1071-412X/04/$08.00+0 DOI: 10.1128/CDLI.11.6.1192-1193.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.
The Biomedical Research Centre, University of British Columbia,1 Department of Pediatrics, British Columbia Children's Hospital, Vancouver, Canada2
Received 26 July 2004/ Returned for modification 20 August 2004/ Accepted 9 September 2004
Hyper-immunoglobulin M (IgM) syndrome (HIGM) is a rare heterogeneous primary immune deficiency. We describe a patient with HIGM characterized by skewed production of serum IgG subclasses and normal somatic hypermutation. This case may represent a subgroup of HIGM type 4 that is characterized by a biased switching to the V-region proximal constant regions.
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