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首页> 外文期刊>BMC Medical Genetics >Associations between speech features and phenotypic severity in Treacher Collins syndrome
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Associations between speech features and phenotypic severity in Treacher Collins syndrome

机译:Treacher Collins综合征的言语特征与表型严重性之间的关联

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Background Treacher Collins syndrome (TCS, OMIM 154500) is a rare congenital disorder of craniofacial development. Characteristic hypoplastic malformations of the ears, zygomatic arch, mandible and pharynx have been described in detail. However, reports on the impact of these malformations on speech are few. Exploring speech features and investigating if speech function is related to phenotypic severity are essential for optimizing follow-up and treatment. Methods Articulation, nasal resonance, voice and intelligibility were examined in 19 individuals (5–74 years, median 34?years) divided into three groups comprising children 5–10 years (n?=?4), adolescents 11–18 years (n?=?4) and adults 29?years and older (n?=?11). A speech composite score (0–6) was calculated to reflect the variability of speech deviations. TCS severity scores of phenotypic expression and total scores of Nordic Orofacial Test-Screening (NOT-S) measuring orofacial dysfunction were used in analyses of correlation with speech characteristics (speech composite scores). Results Children and adolescents presented with significantly higher speech composite scores (median 4, range 1–6) than adults (median 1, range 0–5). Nearly all children and adolescents (6/8) displayed speech deviations of articulation, nasal resonance and voice, while only three adults were identified with multiple speech aberrations. The variability of speech dysfunction in TCS was exhibited by individual combinations of speech deviations in 13/19 participants. The speech composite scores correlated with TCS severity scores and NOT-S total scores. Speech composite scores higher than 4 were associated with cleft palate. The percent of intelligible words in connected speech was significantly lower in children and adolescents (median 77%, range 31–99) than in adults (98%, range 93–100). Intelligibility of speech among the children was markedly inconsistent and clearly affecting the understandability. Conclusions Multiple speech deviations were identified in children, adolescents and a subgroup of adults with TCS. Only children displayed markedly reduced intelligibility. Speech was significantly correlated with phenotypic severity of TCS and orofacial dysfunction. Follow-up and treatment of speech should still be focused on young patients, but some adults with TCS seem to require continuing speech and language pathology services.
机译:背景Treacher Collins综合征(TCS,OMIM 154500)是颅面发育的罕见先天性疾病。详细描述了耳朵,弓,下颌骨和咽部的特征性发育不良畸形。但是,关于这些畸形对语音的影响的报道很少。探索言语特征并研究言语功能是否与表型严重程度相关,对于优化随访和治疗至关重要。方法对19例(5-74岁,中位数34?岁)的人的发音,鼻腔共振,声音和清晰度进行了检查,分为3组,包括5-10岁的儿童(n = 4),青少年11-18岁(n)。 ?=?4)和29岁及以上的成年人(n?=?11)。计算语音综合得分(0-6)以反映语音偏差的变化性。表型表达的TCS严重程度评分和北欧口咽部测试筛查(NOT-S)测量口部功能障碍的总评分用于分析与语音特征的相关性(语音复合评分)。结果儿童和青少年的语音综合得分(中位数4,范围1–6)明显高于成人(中位数1,范围0-5)。几乎所有儿童和青少年(6/8)都表现出发音清晰度,鼻腔共鸣和语音偏差,而只有3名成年人被识别出多种语音异常。在13/19的参与者中,语音偏差的单独组合显示了TCS中语音功能障碍的变异性。语音综合评分与TCS严重程度评分和NOT-S总评分相关。语音综合评分高于4分与c裂相关。儿童和青少年的连接语音中可理解单词的百分比(成人,中位数77%,范围31–99)明显低于成人(98%,范围93-100)。儿童之间的语音清晰度明显不一致,并且明显影响其可理解性。结论在儿童,青少年和成人TCS亚组中发现了多种语言偏向。只有孩子表现出的清晰度明显下降。言语与TCS的表型严重程度和口面功能障碍显着相关。言语的随访和治疗仍应集中在年轻患者上,但是一些患有TCS的成年人似乎需要持续的言语和语言病理服务。

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