Acute Megakaryoblastic Leukemia
What's New
Last Posted: Feb 11, 2023
- Pediatric non-Down syndrome acute megakaryoblastic leukemia is characterized by distinct genomic subsets with varying outcomes.
de Rooij Jasmijn D E, et al. Nature genetics 2017 0 (3) 451-456 - TP53 and PTEN mutations were shared in concurrent germ cell tumor and acute megakaryoblastic leukemia.
Akizuki Keiichi, et al. BMC cancer 2020 0 (1) 5 - Incidence, Survival, and Risk Factors for Adults with Acute Myeloid Leukemia Not Otherwise Specified and Acute Myeloid Leukemia with Recurrent Genetic Abnormalities: Analysis of the Surveillance, Epidemiology, and End Results (SEER) Database, 2001-2013.
Song Xiaolu et al. Acta haematologica 2018 Feb 139(2) 115-127 - Acute Megakaryoblastic Leukemia with Myelodysplasia-related Changes Associated with ATM Gene Deletion.
Ureshino Hiroshi, et al. Internal medicine (Tokyo, Japan) 2016 0 (12) 1625-9 - An Inv(16)(p13.3q24.3)-encoded CBFA2T3-GLIS2 fusion protein defines an aggressive subtype of pediatric acute megakaryoblastic leukemia.
- Acute megakaryoblastic leukemia
From NCATS Genetic and Rare Diseases Information Center - Incidence and clinical implications of GATA1 mutations in newborns with Down syndrome.
Pine Sharon R, et al. Blood 2007 9 (6) 2128-31 - No mutations in the GATA-1 gene detected in patients with acquired essential thrombocythemia.
Gandini Domenica, et al. Haematologica 2004 5 (5) 613-5
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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
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- Page last reviewed:Feb 1, 2024
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