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Autoimmune lymphoproliferative syndrome associated with severe humoral immunodeficiency and monoclonal gammopathy

✍ Scribed by R. Nanan; P. Ströbel; J.-P. Haas; A. Marx; H. Kreth


Publisher
Springer
Year
2002
Tongue
English
Weight
33 KB
Volume
81
Category
Article
ISSN
0939-5555

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## Abstract Autoimmune hemolytic anemia due to warm reactive IgM autoantibodies is unusual, severe, and often fails to respond to standard immunosuppressive therapies in both adults and children. A 6‐year‐old girl with common variable immunodeficiency had longstanding steroid dependent, splenectomy