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Síndrome asociado a MECOM: insuficiencia medular grave sin anomalías esqueléticas, como variante clínica distinta. Reporte de caso
English The MECOM-associated syndrome encompasses a spectrum of hematologic and skeletal abnormalities, with severe bone marrow failure being one of its main manifestations. The case of a seven-month-old male infant, presenting at two months of age with se-vere pancytopenia, is described. Bone marrow stud-ies revealed hypocellularity with poor hematopoietic representation and hypolobulated megakaryocytes, with a normal karyotype (46, XY).
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