先天性巨细胞病毒感染的两个兄弟姐妹的听神经病谱系障碍:两例罕见病例

IF 0.2 Q4 OTORHINOLARYNGOLOGY Indian Journal of Otology Pub Date : 2022-01-01 DOI:10.4103/indianjotol.indianjotol_25_21
R. Suwento, Kartika Hajarani, Semiramis Zizlavsky, T. Airlangga
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引用次数: 0

摘要

听神经病谱系障碍(ANSD)是一种罕见的听觉障碍,当信号在听觉通路上传输中断时。感染是引起ANSD的多因素原因之一。只有少数研究人员报告了由先天性巨细胞病毒(CMV)感染引起的ANSD病例,很少有研究人员报告涉及兄弟姐妹的病例。在我们的研究中,这两名患者是兄弟姐妹,年龄分别为3岁零7个月和8个月。他们早产,有小头畸形;抗CMV IgG水平是反应性的。畸变产物耳声发射测试正常。点击听觉脑干反应显示,在80dB的刺激下没有检测到波,并获得耳蜗微音反应。未观察到中耳异常,并注意到负声反射。计划使用低增益助听器进行听力训练、言语治疗和运动训练,并将患者转诊至儿科神经科进行CMV管理。
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Auditory neuropathy spectrum disorder in two siblings with congenital cytomegalovirus infections: Two rare cases
Auditory neuropathy spectrum disorder (ANSD) is a rare hearing disorder when signal transmission is disrupted on the auditory pathway. Infection is one of the multifactorial causes of ANSD. Only a few researchers have reported the cases of ANSD caused by congenital cytomegalovirus (CMV) infection, and fewer have presented cases involving siblings. In our study, the two patients were siblings, aged 3 years and 7 months and 8 months. They were born prematurely, had microcephaly; anti-CMV IgG levels were reactive. Distortion product otoacoustic emissions test was normal. A click auditory brainstem response showed that no wave was detected with an 80 dB stimulus, and a cochlear microphonic response was obtained. No abnormality in the middle ear was observed, and negative acoustic reflexes were noted. Hearing habilitation with a low-gain hearing aid, speech therapy, and motoric habilitation was planned, and the patients were referred to the pediatric neurology for CMV management.
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来源期刊
Indian Journal of Otology
Indian Journal of Otology OTORHINOLARYNGOLOGY-
CiteScore
0.40
自引率
0.00%
发文量
21
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