Hyper-IgM syndrome is a primary immunodeficiency disorder that is commonly caused by a defect in the CD40 ligand. This defect results in a failure of proper T-cell signaling, leading to defects in immunoglobulin class switching, which is why patients with hyper-IgM syndrome have elevated levels of IgM and low levels of other antibodies. The other listed options are not typically associated with this syndrome.