LIGHD describes the first case of autosomal-recessive ezrin deficiency in a patient with hypogammaglobulinemia and low frequencies of switched memory B, CD4+ and CD8+ T, MAIT, γδ T, and central naive CD4+ cells. The results have been published in “The Journal of Allergy and Clinical Immunology” under the title “Inherited human ezrin deficiency impairs adaptive immunity«.