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沙特阿拉伯镰状细胞病患者的感音神经性听力损失

Sensorineural hearing loss in sickle cell disease patients in Saudi Arabia.

作者信息

Ashoor A, Al-Awamy B

出版信息

Trop Geogr Med. 1985 Dec;37(4):314-8.

PMID:4095769
Abstract

Among the complications of sickle cell disease, sensorineural deafness is well documented in the Western literature; little is known about it in Saudi Arabian patients, in whom the general pattern of the disease has been reported to be "mild," attributed partly to high levels of HbF. The auditory function of 42 patients with sickle cell anemia was evaluated clinically and audiometrically and compared with 27 normal controls. Sensorineural deafness was observed in 10 (23.8%) of our patients.

摘要

在镰状细胞病的并发症中,感音神经性耳聋在西方文献中有充分记载;而在沙特阿拉伯患者中对此了解甚少,据报道该国该疾病的总体模式为“轻度”,部分原因是胎儿血红蛋白(HbF)水平较高。对42例镰状细胞贫血患者的听觉功能进行了临床和听力测定评估,并与27名正常对照者进行了比较。我们的患者中有10例(23.8%)出现了感音神经性耳聋。

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