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Title: GATA2 deficiency: a protean disorder of hematopoiesis, lymphatics, and immunity.
Authors: Spinner MA,  Sanchez LA,  Hsu AP,  Shaw PA,  Zerbe CS,  Calvo KR,  Arthur DC,  Gu W,  Gould CM,  Brewer CC,  Cowen EW,  Freeman AF,  Olivier KN,  Uzel G,  Zelazny AM,  Daub JR,  Spalding CD,  Claypool RJ,  Giri NK,  Alter BP,  Mace EM,  Orange JS,  Cuellar-Rodriguez J,  Hickstein DD,  Holland SM
Journal: Blood
Date: 2014 Feb 6
Branches: CGB
PubMed ID: 24227816
PMC ID: PMC3916876
Abstract: Haploinsufficiency of the hematopoietic transcription factor GATA2 underlies monocytopenia and mycobacterial infections; dendritic cell, monocyte, B, and natural killer (NK) lymphoid deficiency; familial myelodysplastic syndromes (MDS)/acute myeloid leukemia (AML); and Emberger syndrome (primary lymphedema with MDS). A comprehensive examination of the clinical features of GATA2 deficiency is currently lacking. We reviewed the medical records of 57 patients with GATA2 deficiency evaluated at the National Institutes of Health from January 1, 1992, to March 1, 2013, and categorized mutations as missense, null, or regulatory to identify genotype-phenotype associations. We identified a broad spectrum of disease: hematologic (MDS 84%, AML 14%, chronic myelomonocytic leukemia 8%), infectious (severe viral 70%, disseminated mycobacterial 53%, and invasive fungal infections 16%), pulmonary (diffusion 79% and ventilatory defects 63%, pulmonary alveolar proteinosis 18%, pulmonary arterial hypertension 9%), dermatologic (warts 53%, panniculitis 30%), neoplastic (human papillomavirus+ tumors 35%, Epstein-Barr virus+ tumors 4%), vascular/lymphatic (venous thrombosis 25%, lymphedema 11%), sensorineural hearing loss 76%, miscarriage 33%, and hypothyroidism 14%. Viral infections and lymphedema were more common in individuals with null mutations (P = .038 and P = .006, respectively). Monocytopenia, B, NK, and CD4 lymphocytopenia correlated with the presence of disease (P < .001). GATA2 deficiency unites susceptibility to MDS/AML, immunodeficiency, pulmonary disease, and vascular/lymphatic dysfunction. Early genetic diagnosis is critical to direct clinical management, preventive care, and family screening.