对一例罕见综合征患者进行言语治疗干预的结果:案例研究

Belén Valverde, Marta Rodríguez, Lorena García, Teresa Simón, Miguel Lázaro
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引用次数: 0

摘要

在本研究中,我们介绍了对一名患有罕见疾病(13q11q12.12 部分四体综合征)的儿童进行言语和语言治疗干预的结果。在患儿 4 岁时,我们对其进行了首次评估(T1),并设定了治疗目标。治疗开始 6 个月后,对患儿进行重新评估(T2),并设计新的特定干预方案。治疗 6 个月后,再次对患儿进行评估,以了解可能取得的进展(T3)。干预结果表明,在 T1 和 T2 期 间,儿童在注意力保持和交流意图等所有语言先决条件方面都取得了明显的进步。同样,在 T2 和 T3 之间,尽管上述语言先决条件也有明显改善,但最大的进步体现在语言表达能力的发展上。我们将根据以往对罕见遗传病患者进行的少数研究来讨论这些结果。
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Resultados de la intervención logopédica en un caso de síndrome raro: un estudio de caso

In this study we present the results of a speech and language therapy intervention in a case of a child with a rare disease -partial tetrasomy 13q11q12.12. At the age of 4, a first evaluation is performed (T1), and treatment goals are set. Six months after the beginning of the treatment, the child is re-evaluated (T2) and a new specific intervention program is designed. After another 6 months of treatment, the child is evaluated again in order to know the possible progress experienced (T3). The results of the intervention show a clear progression between T1 and T2 in all the linguistic prerequisites worked on, such as attention maintenance and communicative intention. Likewise, between T2 and T3, the greatest progress is observed in the development of expressive language, although notable improvements in the aforementioned linguistic prerequisites can also be observed. These results are discussed in the light of the few previous existing studies with patients with rare genetic diseases.

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