Transient hypogammaglobulinemia of infancy is characterized as a reduction of one or more classes of immunoglobulins with a response to vaccines and normal subpopulations of lymphocytes B presenting in the first years of life. The diagnosis is made a posteriori, once the levels of immunoglobulins are normalized, in general between 2 and 4 years of age. Clinical presentation varies : The child may be either asymptomatic or present with recurrent infections, atopy and / or auto-immunity. There are no clinical or immunological features that distinguish this condition from a common variable immunodeficiency (CVID). Because of the risk of severe infections, it is necessary a follow up by a paediatric immunologist. Depending on the presentation and evolution, a prophylaxis with antibiotics or a substitution with immunoglobulins might be indicated.

Enders F.B., Conti F., Candotti F., Angelini T.F. (2017). Transient hypogammaglobulinemia of infancy. REVUE MÉDICALE SUISSE, 13(557), 1-4.

Transient hypogammaglobulinemia of infancy

Conti F.;
2017

Abstract

Transient hypogammaglobulinemia of infancy is characterized as a reduction of one or more classes of immunoglobulins with a response to vaccines and normal subpopulations of lymphocytes B presenting in the first years of life. The diagnosis is made a posteriori, once the levels of immunoglobulins are normalized, in general between 2 and 4 years of age. Clinical presentation varies : The child may be either asymptomatic or present with recurrent infections, atopy and / or auto-immunity. There are no clinical or immunological features that distinguish this condition from a common variable immunodeficiency (CVID). Because of the risk of severe infections, it is necessary a follow up by a paediatric immunologist. Depending on the presentation and evolution, a prophylaxis with antibiotics or a substitution with immunoglobulins might be indicated.
2017
Enders F.B., Conti F., Candotti F., Angelini T.F. (2017). Transient hypogammaglobulinemia of infancy. REVUE MÉDICALE SUISSE, 13(557), 1-4.
Enders F.B.; Conti F.; Candotti F.; Angelini T.F.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/950740
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