儿童遗传性溶血性贫血

Şefika Akyol, Akif Tahiroğlu, E. Unal
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引用次数: 0

摘要

遗传性溶血性贫血是儿科最常见的贫血之一,尤其是在近亲婚姻很常见的土耳其。遗传性溶血性贫血主要包括血红蛋白病、红细胞膜缺陷和酶缺陷。溶血性贫血有广泛的病因和临床谱,获得性和遗传性的原因在儿童。总是仔细的自我和家族史回顾和综合体检和实验室结果是鉴别诊断至关重要。因此,医生应掌握预防方法和早期诊断指标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inherited hemolytic anemias in children
Inherited hemolytic anemia is one of the most commonly seen anemias encountred in the pediatric age, especially in Türkiye, where consanguineous marriages are common. Inherited hemolytic anemias mainly includes hemoglobinopathies, erythrocyte membrane defects and enzyme defects. Hemolytic anemias have a wide etiology and clinical spectrum with acquired and hereditary causes in childhood. Always a careful self and family history review and synthesis of physical examination and laboratory findings are vital for differential diagnosis. Therefore, physicians should be competent about prevention methods and early diagnosis markers.
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