Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition A rare, genetic, primary combined T and B cell immunodeficiency characterized by recurrent, severe viral and bacterial infections. Immunologic findings include decreased immunoglobulin levels, decreased numbers of B and NK cells, reduced relative CD19+ B cells in peripheral blood, impaired memory responses to viral infections and defective antigen-specific T-cell proliferation. Disease data Classification Disease Synonyms Primary immunodeficiency with multifaceted aberrant lymphoid immunity Primary immunodeficiency with multifaceted aberrant lymphoid immunity ORPHA code 447731 OMIM code - ICD10 code D81.8 ICD11 code - *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl