Ballas S K
Cardeza Foundation for Hematologic Research, Department of Medicine, Thomas Jefferson University, Philadelphia, PA 19107.
Ann Clin Lab Sci. 1992 Jul-Aug;22(4):226-8.
A 22-year-old female with factitious sickle cell anemia and recurrent painful crises is described. Because she had sickle cell trait and iron deficiency anemia, she could successfully feign the symptoms of homozygous sickle cell anemia. The identification of this syndrome in patients with genetic disorders is presented.
本文描述了一名患有假性镰状细胞贫血并反复出现疼痛危象的22岁女性。由于她具有镰状细胞性状和缺铁性贫血,她能够成功伪装纯合子镰状细胞贫血的症状。文中介绍了在患有遗传疾病的患者中识别这种综合征的情况。