Syntactic Networks as an Endophenotype of Developmental Language Disorders: An Evo-Devo Approach to Clinical Linguistics

IF 0.6 0 LANGUAGE & LINGUISTICS
L. Barceló-Coblijn, A. Benítez‐Burraco, Aritz Irurtzun
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引用次数: 3

Abstract

Usually, developmental language disorders are defined either symptomatically (based on a constellation of linguistic deficits appearing recurrently within a population) or etiologically (on the basis of a common underlying deficit), or both. On paper, each of these clinical categories is expected to be distinguished from other close entities at several levels of analysis (phenotypic, cognitive, neurobiological, genetic, etc.). Nonetheless, this is not typically the case: Comorbidity, variability, and heterogeneity are in fact a common outcome of the clinical practice. Ultimately, different disorders may share the same underlying deficit (e.g., phonological dysfunction in dyslexia and SLI); conversely, different deficits may give rise to the same disorder (e.g., both visual problems and phonological deficits may contribute to dyslexia) (Benitez-Burraco 2013). If we want to achieve a better—and earlier—diagnosis of these conditions, we should improve the tools we employ at present. A promising approach is one relying on the endophenotypes of disorders. Endophenotypes may be defined as cognitive, neuroanatomical, neurophysiological, endocrine, or biochemical quantifiable components of the space between genes and diseases (Gould & Gottesman 2006). Endophenotypes refer to more specific (and more physiological) aspects of the body function, therefore they allow us to gain a more accurate diagnosis of its dysfunction (Gottesman & Gould 2003). Here we would like to advance a putative endophenotype of language disorders that combines four factors: (1) linguistic analysis (syntactic computation), (2) information management (communicative strategies), (3) recent evo-devo insights in the nature of phenotypic variation, and (4) network approaches to emergent properties of complex systems (surely, language it is; Deacon 2005). To begin with, we would like to note that, although the set of pathological conditions already described by clinical linguists is ample, it is not unlimited either. In other words, variation is constrained or canalized, even in pathological states. At the same time, we observe that language is both sensitive to damage (e.g., some aspects of language processing are perturbed in nearly all disorders, like the proper use of inflectional cues in verbal and nominal morphology) and resistant to perturbation (e.g., a nearly functional language faculty may emerge at the term of growth in spite of severe underlying deficits).
句法网络作为发展性语言障碍的内表型:临床语言学的演化-发展方法
通常,发展性语言障碍的定义要么是症状性的(基于人群中反复出现的语言缺陷的集合),要么是病因性的(基于共同的潜在缺陷),或者两者兼而有之。在纸面上,这些临床类别中的每一个都应该在几个分析水平(表型、认知、神经生物学、遗传等)上与其他接近的实体区分开来。然而,这并不是典型的情况:合并症、变异性和异质性实际上是临床实践的共同结果。最终,不同的障碍可能具有相同的潜在缺陷(例如,阅读障碍和特殊语言障碍的语音功能障碍);相反,不同的缺陷可能导致相同的障碍(例如,视觉问题和语音缺陷都可能导致阅读障碍)(Benitez-Burraco 2013)。如果我们想更好、更早地诊断这些疾病,我们就应该改进我们目前使用的工具。一种有希望的方法是依赖于疾病的内表型。内表型可以定义为基因和疾病之间空间的认知、神经解剖、神经生理、内分泌或生化可量化的组成部分(Gould & Gottesman 2006)。内表型指的是身体功能更具体(和更生理)的方面,因此它们使我们能够更准确地诊断其功能障碍(Gottesman & Gould 2003)。在这里,我们想提出一种假定的语言障碍的内表型,它结合了四个因素:(1)语言分析(句法计算),(2)信息管理(交际策略),(3)最近对表型变异本质的进化-发展见解,以及(4)复杂系统(当然,语言是;2005年执事)。首先,我们想指出,尽管临床语言学家已经描述的病理条件是充分的,但它也不是无限的。换句话说,即使在病理状态下,变异也受到限制或受到控制。同时,我们观察到语言对损伤既敏感(例如,语言处理的某些方面在几乎所有障碍中都受到干扰,例如在言语和名义形态中适当使用屈折线索),又抵抗扰动(例如,尽管存在严重的潜在缺陷,但在生长过程中可能会出现一种近乎功能性的语言能力)。
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来源期刊
Biolinguistics
Biolinguistics LANGUAGE & LINGUISTICS-
CiteScore
1.50
自引率
0.00%
发文量
5
审稿时长
12 weeks
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