STAT1 and Bruton-type agammaglobulinemia: Additionally, there were two patients with CVID, one patient with X-linked agammaglobulinemia (XLA), three patients with hemophagocytic lymphohistiocytosis (HLH), one patient with a defect of innate immunity (i.e., biallelic STAT1 loss-of-function), one patient with a secondary immunodeficiency (lymphopenia), most likely due to severe malnutrition, and one patient with an IgG2 and IgA deficiency without a genetic explanation.