Hyper-IgM syndrome is a rare combined immune deficiency linked to a mutation most frequently found in CD40.The diagnosis is usually made in the presence of recurrent infections, particularly pulmonary, digestive and others. Through to the dosage of lymphocyte subpopulations and after elimination of other differential diagnoses, the diagnosis of hyper-IgM syndrome can be confirmed.
Alan : Sosyal, Beşeri ve İdari Bilimler
Dergi Türü : Uluslararası
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