胺反应性巨芽细胞贫血综合征与新型化合物异性SLC19A2突变和血栓事件:一个病例报告

Francisco Xavier Jiménez1, Carlos Rojas1, Heidi A Fernandez2

  • 1Department of Internal Medicine, Hospital de Especialidades Eugenio Espejo, Quito, Ecuador.

PubMed
概括

胺反应性大球质贫血 (TRMA) 是一种罕见的遗传疾病. 这个案例突出了新的SLC19A2突变和血栓形成,强调早期的胺治疗改善了结果.

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