... XLP) includes the following hereditary and acquired disorders: Common variable immunodeficiency and other hereditary disorders with immunodeficiency (See Table ...

... is caused by biallelic pathogenic variants in FADD . Common variable immunodeficiency 9 (PRKCD deficiency) (OMIM 615559 ). PRKCD deficiency is ... Chevret S, Debré P, Schmitt C, Oksenhendler E. Common variable immunodeficiency patient classification based on impaired B cell memory ...

... TNFSF12 21 TNFRSF13B 22 TNFRSF13C 23 TRNT1 24 Common variable immunodeficiency AD AR Recurrent lung, sinus, & ear infection; recurrent ... of rare and low-frequency genetic variants in common variable immunodeficiency (CVID). Sci Rep. 2021;11:8308. [ PMC free ...

... can have a presentation similar to HIGM1 or common variable immunodeficiency [ Hollenbaugh et al 1994 , de Saint Basile et ... IL21 IRF2BP2 LRBA MS4A1 NFKB1 NFKB2 TNFRSF13B TNFRSF13C Common variable immunodeficiency (CVID) (OMIM PS607594 ) AR AD Recurrent sinopulmonary infections ↓ ...

... al 2018 , Sheppard et al 2021 ]: Immunodeficiency, including common variable immunodeficiency Insufficient response to vaccinations History of recurrent infections ...

... individuals with antibody deficiency and/or features of common variable immunodeficiency, eleven individuals were found to have DADA2 [ Schepp ... CVID. About 5%-6% of individuals diagnosed with common variable immunodeficiency (CVID) and antibody deficiency were found to have ...

... significance of duodenal mucosal atrophy in patients with common variable immunodeficiency: a clinical and histopathologic study. Am J Clin ... and DQ8 in dissecting celiac-like disease in common variable immunodeficiency. J Clin Immunol. 2013 Jul; 33 (5):909– ...

... lactose intolerance, pancreatic exocrine dysfunction, microscopic colitis and common variable immunodeficiency. g. Management of refractory coeliac disease, for example, ...