[微锥细胞性贫血的骨关节受累]。

L De Palma, F Tamburrelli
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引用次数: 0

摘要

Drepanocytosis是一种遗传性血红蛋白病,在黑人中尤为常见;在其纯合子形式中,骨关节系统经常普遍受累,具有清晰可识别的临床和放射图像。微锥细胞增多症(双杂合子)更难识别。根据他们的观察,作者报告了骨科感兴趣的疾病的几个具体方面。
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[Osteo-articular involvement in microdrepanocytic anemia].

Drepanocytosis is a hereditary hemoglobinopathy which is particularly common in Blacks; in its homozygote form there is constant general involvement of the osteoarticular system with clearly recognisable clinical and radiographic pictures. Microdrepanocytosis (double heterozygotosis) is instead more difficult to recognise. Based on their observations the authors report several specific aspects of the disease of orthopaedic interest.

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