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PedAM

Pediatric Disease Annotations & Medicines




Disease leukemia
Phenotype C0013080|trisomy 21
Sentences 8
PubMedID- 25302938 Acute megakaryoblastic leukemia associated with trisomy 21 demonstrates a distinct immunophenotype.
PubMedID- 22513796 [gata1-mutation associated leukemia in children with trisomy 21 mosaic].
PubMedID- 25266042 Acute megakaryoblastic leukemia with acquired trisomy 21 and gata1 mutations in phenotypically normal children.
PubMedID- 25361478 Acute megakaryoblastic leukemia associated with trisomy 21 demonstrates a distinct immunophenotype.
PubMedID- 23467713 One case of acute megakaryoblastic leukemia (amkl) with trisomy 21, trisomy 14 and unmutated gata1 gene in a phenotypically normal girl was reported.
PubMedID- 24396488 The current report presents the first case of saa preceding acute monocytic leukemia (aml-m5) with acquired trisomy 21. written informed consent was obtained from the patient’s family.
PubMedID- 21592571 Cd7-positive acute myelomonocytic leukemia with trisomy 21 as a sole acquired chromosomal abnormality in two adolescents.
PubMedID- 22176774 [10] explained the involvement of gata-binding factor 1 (gata1) mutations in causing transient leukemia in cases with trisomy 21. transient leukemia-related blasts have the potential to grow and differentiate towards particular hematopoietic lineages in the presence of specific hematopoietic growth factors.

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