B cell expansion with NF-κB and T cell anergy (BENTA) is a rare primary immunodeficiency disorder caused by mutations in the CARD11 gene and results in constitutive NF-κB activation in B and T cells. Affected patients present with polyclonal expansion of B cells at an early age with splenomegaly, lymphadenopathy, and mild autoimmunity. Here, we discuss four BENTA cases with unusual clinical manifestations not previously reported. All patients showed previously reported gain-of-function mutations (G123S, G123D, and C49Y) in the CARD11 gene. Severe autoimmune manifestations were noted for the first time in all our patients
Agammaglobulinemia is a rare inherited immunodeficiency disorder. Mutations in the BLNK gene cause l...
Most genetic defects that arrest B-cell development in the bone marrow present early in life with ag...
Mendelian primary immunodeficiency diseases (MPIDs) are rare disorders affecting distinct constituen...
B cell expansion with NF-κB and T cell anergy (BENTA) is a rare primary immunodeficiency disorder ca...
Germline gain-of-function mutations in CARD11 lead to the primary immunodeficiency, B cell expansion...
CARD11 is a lymphocyte-specific scaffold molecule required for proper activation of B- and T-cells i...
CARD11 is a lymphocyte-specific scaffold molecule required for proper activation of B- and T-cells i...
The antigen receptors of lymphocytes are coupled to signaling pathways which are essential for B cel...
CBL syndrome is a Noonan-like RASopathy with heterogeneous clinical phenotype and predisposition to ...
CARD11 encodes a scaffold protein in lymphocytes that links antigen receptor engagement with downstr...
Thesis (Ph.D.)--University of Washington, 2018Gain of function mutations in key signaling molecules ...
Mendelian Primary Immunodeficiency Diseases (MPIDs) are rare disorders affecting distinct constituen...
Non-canonical NF-κB-pathway signaling is integral in immunoregulation. Heterozygous mutations in NFK...
We described for the first time a female patient with the simultaneous presence of two homozygous mu...
Common variable immunodeficiency (CVID) is a heterogeneous disorder characterized by antibody defici...
Agammaglobulinemia is a rare inherited immunodeficiency disorder. Mutations in the BLNK gene cause l...
Most genetic defects that arrest B-cell development in the bone marrow present early in life with ag...
Mendelian primary immunodeficiency diseases (MPIDs) are rare disorders affecting distinct constituen...
B cell expansion with NF-κB and T cell anergy (BENTA) is a rare primary immunodeficiency disorder ca...
Germline gain-of-function mutations in CARD11 lead to the primary immunodeficiency, B cell expansion...
CARD11 is a lymphocyte-specific scaffold molecule required for proper activation of B- and T-cells i...
CARD11 is a lymphocyte-specific scaffold molecule required for proper activation of B- and T-cells i...
The antigen receptors of lymphocytes are coupled to signaling pathways which are essential for B cel...
CBL syndrome is a Noonan-like RASopathy with heterogeneous clinical phenotype and predisposition to ...
CARD11 encodes a scaffold protein in lymphocytes that links antigen receptor engagement with downstr...
Thesis (Ph.D.)--University of Washington, 2018Gain of function mutations in key signaling molecules ...
Mendelian Primary Immunodeficiency Diseases (MPIDs) are rare disorders affecting distinct constituen...
Non-canonical NF-κB-pathway signaling is integral in immunoregulation. Heterozygous mutations in NFK...
We described for the first time a female patient with the simultaneous presence of two homozygous mu...
Common variable immunodeficiency (CVID) is a heterogeneous disorder characterized by antibody defici...
Agammaglobulinemia is a rare inherited immunodeficiency disorder. Mutations in the BLNK gene cause l...
Most genetic defects that arrest B-cell development in the bone marrow present early in life with ag...
Mendelian primary immunodeficiency diseases (MPIDs) are rare disorders affecting distinct constituen...