| Literature DB >> 8339007 |
T Ohzeki1, K Hanaki, H Motozumi, H Ohtahara, H Hayashibara, Y Harada, M Okamoto, K Shiraki, Y Tsuji, H Emura.
Abstract
Growth hormone deficiency associated with hypogammaglobulinemia has been reported only in a few publications. Our patient was a male with recurrent episodes of infections. Serum immunoglobulin (Ig) G was extremely low although IgM concentration was much greater than the normal limit. Growth hormone responses to insulin, 1-Dopa and growth hormone-releasing hormone were low. The mean growth hormone concentration during sleep was less than the normal limit. These results are consistent with hyper-IgM immunodeficiency associated with growth hormone deficiency. The mode of transmission appears to be autosomal dominant. This combination has not been reported previously.Entities:
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Year: 1993 PMID: 8339007 DOI: 10.1111/j.1651-2227.1993.tb12773.x
Source DB: PubMed Journal: Acta Paediatr ISSN: 0803-5253 Impact factor: 2.299