پديد آورندگان :
Safari Mojgan نويسنده , Rezaei Nima نويسنده , Hajiloot Mehrdad نويسنده , Pan-Hammarstrom Qiang نويسنده , Hammarstrom Lennart نويسنده
چكيده لاتين :
Immunoglobulin class switch recombination deficiencies (Ig CSR deficiencies) or Hyper
IgM syndromes (HIGM) are a group of primary immunodeficiency diseases, characterized by
defective CD40 signaling of B cells, resulting in reduced CSR and somatic hypermutation.
The affected patients are characterized by low serum levels of IgG and IgA, and normal or
elevated levels of IgM, which lead to an increased susceptibility to infections.
We describe a 3 year-old boy with frequent bacterial infections of the skin and respiratory
tract, mucosal ulcers, and diarrhea. He experienced onychomadesis of both fingernails and
toenails during a recent bacterial infection. Quantitative immunoglobulin measurements
revealed high levels of serum IgM and very low levels of IgG, IgA, and IgE. Clinical and
immunologic studies supported the diagnosis of HIGM.
Exclusion of CD40L, CD40, AID and UNG genes by molecular analysis in this patient
may suggest a new form of selective CSR deficiency.