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对患有遗传性弹性蛋白基因异常个体的嗓音质量调查。

An investigation of voice quality in individuals with inherited elastin gene abnormalities.

作者信息

Watts Christopher R, Awan Shaheen N, Marler Jeffrey A

机构信息

Department of Communication Sciences & Disorders, James Madison University, VA 22807, USA.

出版信息

Clin Linguist Phon. 2008 Mar;22(3):199-213. doi: 10.1080/02699200701803361.

Abstract

The human elastin gene (ELN) is responsible for the generation of elastic fibres in the extracellular matrix of connective tissue throughout the body, including the vocal folds. Individuals with Supravalvular aortic stenosis (SVAS) and Williams syndrome (WS) lack one normal ELN allele due to heterozygous ELN abnormalities, resulting in a haploinsufficiency. We measured perceptual and acoustic characteristics of voice quality in individuals with SVAS and WS to investigate the consequences to vocal function secondary to ELN haploinsufficiency. Results indicated that the voice quality of individuals with SVAS/WS was rated as significantly more abnormal, rough, and hoarse compared to normal controls, and that adults with SVAS/WS were rated as significantly lower in pitch. Acoustic measures indicated that individuals with SVAS/WS produced greater instability of fundamental frequency during phonation (as reflected via increased pitch sigma and increased jitter). These findings support the possibility that heterozygous ELN abnormalities negatively influence vocal fold biomechanics and the resulting sound produced by the vibrating glottis.

摘要

人类弹性蛋白基因(ELN)负责在包括声带在内的全身结缔组织细胞外基质中生成弹性纤维。患有主动脉瓣上狭窄(SVAS)和威廉姆斯综合征(WS)的个体由于杂合性ELN异常而缺少一个正常的ELN等位基因,导致单倍剂量不足。我们测量了患有SVAS和WS的个体的嗓音质量的感知和声学特征,以研究ELN单倍剂量不足对发声功能的影响。结果表明,与正常对照组相比,患有SVAS/WS的个体的嗓音质量被评定为明显更异常、粗糙和嘶哑,并且患有SVAS/WS的成年人的音高被评定为明显更低。声学测量表明,患有SVAS/WS的个体在发声过程中产生的基频稳定性更高(通过音高标准差增加和抖动增加反映)。这些发现支持了杂合性ELN异常对声带生物力学以及振动声门产生的声音产生负面影响的可能性。

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