Gata2 Deficiency
What's New
Last Posted: Dec 30, 2023
- Genetic Characteristics of Patients with Young-Onset Myelodysplastic Neoplasms.
Hyun-Young Kim, et al. Journal of clinical medicine 2023 0 (24) - Gata2 Noncoding Genetic Variation as a Determinant of Hematopoietic Stem/Progenitor Cell Mobilization Efficiency.
Alexandra A Soukup, et al. Blood advances 2023 0 - Prevalence and clinical expression of germline predisposition to myeloid neoplasms in adults with marrow hypocellularity.
Elisabetta Molteni, et al. Blood 2023 0 - The Clinical Spectrum, Diagnosis, and Management of GATA2 Deficiency.
Marta Santiago et al. Cancers 2023 15(5) - Lethal Influenza in Two Related Adults with Inherited GATA2 Deficiency.
Sologuren Ithaisa, et al. Journal of clinical immunology 2018 0 (4) 513-526 - ASXL1 and STAG2 are common mutations in GATA2 deficiency patients with bone marrow disease and myelodysplastic syndrome.
West Robert R, et al. Blood advances 2021 0 (3) 793-807 - Somatic GATA2 mutations define a subgroup of myeloid malignancy patients at high risk for invasive fungal disease.
Vedula Rahul S, et al. Blood advances 2021 0 (1) 54-60 - Monitoring and treatment of MDS in genetically susceptible persons.
Davies Stella M et al. Hematology. American Society of Hematology. Education Program 2019 2019(1) 105-109 - Old and new tools in the clinical diagnosis of inherited bone marrow failure syndromes.
West Allison H et al. Hematology. American Society of Hematology. Education Program 2017 2017(1) 79-87 - Acquired and germline predisposition to bone marrow failure: Diagnostic features and clinical implications.
Kallen Michael E et al. Seminars in hematology 2019 56(1) 69-82
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Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
- Page last updated:May 01, 2024
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