Choroba BENTA

Kod Orpha: 464336Kod OMIM: 616452

Definicja

A rare primary immunodeficiency characterized by infantile onset of generalized lymphadenopathy, splenomegaly, and lymphocytosis, with excessive polyclonal expansion of B-cells. Patients present recurrent infections and impaired T-cell and antibody responses, while overt autoimmune manifestations are usually absent. Occurrence of B-cell malignancy later in life has been reported.

Dane
Klasyfikacja

Choroba

Synonimy
B-cell expansion with NF-kB and T-cell anergy disease
B-cell expansion with NF-kB and T-cell anergy disease
Kod ORPHA
464336
Kod OMIM
616452
Kod ICD10
D81.8
Kod ICD11
-

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