Disease | pancytopenia |
Comorbidity | C0030312|pancytopenia |
Sentences | 8 |
PubMedID- 23908116 | Congenital amegakaryocytic thrombocytopenia (camt) is caused by the loss of thrombopoietin receptor-mediated (mpl-mediated) signaling, which causes severe pancytopenia leading to bone marrow failure with onset of thrombocytopenia and anemia prior to leukopenia. |
PubMedID- 25687089 | Aplastic anemia(aa) is a disease,including congenital aa and acquired aa, characterized by an extremely hypocellular marrow and peripheral blood pancytopenia due to bone marrow failure. |
PubMedID- 20301575 | Progressive bone marrow failure with pancytopenia typically presents in the first decade, often initially with thrombocytopenia or leukopenia. |
PubMedID- 24505406 | Aplastic anemia (aa) is a hematologic disease characterized by peripheral pancytopenia with bone marrow failure, and has the absence of an abnormal infiltrates and no increase in reticulin. |
PubMedID- 26435988 | Paroxysmal nocturnal haemoglobinuria (pnh) is a rare type of acquired haemolytic anaemia that is described as a triad of acquired intravascular haemolysis, venous thrombosis and anaemia with pancytopenia sometimes due to bone marrow failure. |
PubMedID- 24187634 | Case reports have suggested that hypothermia can also cause bone marrow failure leading to pancytopenia [27]. |
PubMedID- 25728776 | Additionally, in contrast to individuals with lig4 mutations, pancytopenia leading to bone marrow failure has not been observed. |
PubMedID- 20618967 | This treatment is followed by a period of severe bone marrow failure with severe pancytopenia, including lymphopenia. |
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