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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




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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