%0 Generic %A B., Egenlauf %A M., Schuhmann %A T., Giese %A T., Junghanss %A M., Stojkovic %A K., Tintelnot %A S., deHoog %A J., Greil %A E., Richter %A M., Vehresschild %A C.P., Heussel %A F.J.F., Herth %A M., Kreuter %D 2019 %T Supplementary Material for: Disseminated Mycosis by Arthrocladium fulminans Jeopardizing a Patient with GATA2 Deficiency %U https://karger.figshare.com/articles/dataset/Supplementary_Material_for_Disseminated_Mycosis_by_b_i_Arthrocladium_i_b_b_i_fulminans_i_b_Jeopardizing_a_Patient_with_GATA2_Deficiency/7916417 %R 10.6084/m9.figshare.7916417.v1 %2 https://karger.figshare.com/ndownloader/files/14740130 %K Arthrocladium fulminans %K Melanized fungus %K MonoMAC %K Immunodeficiency syndrome %K GATA2 %K Mycobacterium sherrisii %X GATA2 deficiency is characterized by monocytopenia, deficiency of dendritic cells, and a variable degree of lymphocytopenia affecting B cells and NK cells, leading to an enhanced risk of mycobacterial, viral, and fungal infections. Here we present a patient with a heterozygous intronic GATA2 mutation who acquired a fatal disseminated mycosis due to the black yeast-like fungus Arthrocladium fulminans following an infection with Mycobacterium sherrisii. This case illustrates that in patients with severe uncommon infections, immunodeficiency syndromes must be ruled out. %I Karger Publishers