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一名患有布朗-维阿莱托-范莱尔综合征的男性耳聋后病程迁延。

Protracted disease course after deafness in a man with Brown-Vialetto-Van Laere syndrome.

作者信息

Yadegari Samira, Razmjoo Keyvan, Nafissi Shahriar

机构信息

Department of Neurology, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Neurosciences (Riyadh). 2012 Jul;17(3):253-5.

Abstract

Brown-Vialetto-Van Laere syndrome (BVVLS) is a rare type of motor neuron disease, characterized by bilateral deafness, and multiple cranial nerve involvement. The disease is more frequent in females, but rapid deterioration was attributed to male gender or early onset. Herein, we report a man with BVVLS who had a longer than expected interval between onset of deafness and other motor symptoms that culminated to diagnosis. Six years later, he had gradual worsening and death. Along with potential new developing therapeutic options, this case emphasizes considering the diagnosis of BVVLS especially after a long period of stability, even in men.

摘要

布朗-维阿莱托-范莱尔综合征(BVVLS)是一种罕见的运动神经元疾病,其特征为双侧耳聋和多组颅神经受累。该疾病在女性中更为常见,但病情快速恶化归因于男性性别或发病较早。在此,我们报告一名患有BVVLS的男性患者,其耳聋发作与最终确诊的其他运动症状之间的间隔时间比预期更长。六年后,他病情逐渐恶化并死亡。随着潜在新治疗方案的出现,该病例强调即使在男性患者中,尤其是在长期病情稳定后,也应考虑BVVLS的诊断。

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