偶尔在一个有声障碍的青少年中诊断出交叉性异常性半高:一个病例报告
相关实验视频
Updated: Jun 18, 2025

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Full-Endoscopic Surgery for Hypothalamic Hamartoma Resection
Published on: April 12, 2024
303
Lei Dong1, Shasha Kang1, Xiumei Chen1
1Department of Otorhinolaryngology Head and Neck Surgery, Yantai Yuhuangding Hospital, Shandong University, China.
Heliyon
|July 29, 2024
概括
异常性半高缩 (HH) 可能导致先天性喉不对称和语音障碍. 语音正疗法有效地改善了不适合手术的患者的症状.
科学领域:
- 医学遗传学 医学遗传学
- 耳鼻喉科 耳鼻喉科 耳鼻喉科
- 儿科 儿科 儿科
背景情况:
- 血高缩 (HH) 是一种罕见的先天性疾病,其特点是身体或四肢不对称的过度生长,通常在出生时被诊断出来.
- 高血压可以表现为美学和移动性问题,在某些情况下,与瘤或发育异常有关.
研究的目的:
- 报告一种由异常性半高缩引起的语音障碍病例.
- 突出语音纠正疗法作为治疗HH相关的语音问题.
主要方法:
- 一个14岁男孩的案例介绍,自婴儿时期以来一直声.
- 喉腔镜检查,CT扫描和语音分析,以评估喉结构和功能.
- 根据患者的年龄和生长阶段实施的个性化语音校正疗法.
主要成果:
- 喉检查显示了双边不对称性,与交叉异常性HH一致.
- 被诊断出严重的声音障碍.
- 在语音纠正治疗后,观察到声音障碍的显著改善.
结论:
- kongenital hemihypertrophy可能导致喉不对称以及随后的语音障碍.
- 语音正疗法为患有HH相关语音问题的患者提供了一种有效的治疗选择,这些患者不是手术候选人.
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