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Immunologic studies of three family members with the immunodeficiency with hyper-IgM syndrome

✍ Scribed by Zacharie Brahmi; Kenneth H. Lazarus; M. E. Hodes; Robert L. Baehner

Publisher
Springer
Year
1983
Tongue
English
Weight
980 KB
Volume
3
Category
Article
ISSN
0271-9142

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Hyper-IgM (HIM) syndrome is a rare primary immunodeficiency disorder. Approximately 120 cases have been described in the literature world-wide. Features of HIM include low serum IgG, a very low IgA with normal or high IgM levels. Autoimmune phenomena are recognized associations but connective tissue