Evidence map›Paper›PMID 40664354›Full record

ArticleJournal of speech, language, and hearing research : JSLHR2025

Prelinguistic Communication Complexity of Children With Neurogenetic Syndromes.

Lisa R Hamrick, Olivia Boorom, Katiana Estrada, Nancy Brady, Bridgette Kelleher

Abstract read
In one paragraph

Article in Journal of speech, language, and hearing research : JSLHR, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Lisa R HamrickDepartment of Psychology, University of South Carolina, Columbia.ORCID 0000-0002-8372-5837
Olivia BooromDepartment of Speech-Language-Hearing: Sciences and Disorders, The University of Kansas, Lawrence.ORCID 0000-0003-4970-7368
Katiana EstradaDepartment of Psychological Sciences, Purdue University, Lafayette, IN.ORCID 0000-0002-3269-2246
Nancy BradyDepartment of Speech-Language-Hearing: Sciences and Disorders, The University of Kansas, Lawrence.ORCID 0000-0001-7573-9000
Bridgette KelleherDepartment of Psychological Sciences, Purdue University, Lafayette, IN.ORCID 0000-0001-7966-1837

Funding

The Effects of Parenting on the Development and Behavior of Adolescents with FXSR01HD084563 · NICHD · UNIVERSITY OF KANSAS LAWRENCE · PI NANCY CAROLINE BRADY · 2016 to 2026
$4.7M
Discovering novel predictors of minimally verbal outcomes in autism through computational modelingR01DC020048 · NIDCD · GEORGIA INSTITUTE OF TECHNOLOGY · PI NANCY CAROLINE BRADY, Agata Rozga · 2022 to 2026
$2.6M
Telehealth Assessment of Syndromic Autism Risk in InfantsK23MH111955 · NIMH · PURDUE UNIVERSITY · PI KELLEHER, BRIDGETTE LYNNE · 2017 to 2021
$913k
Analysis of early vocalization features in children at high genetic risk for autismF31DC018219 · NIDCD · PURDUE UNIVERSITY · PI HAMRICK, LISA M · 2019 to 2021
$117k
NICHD NIH HHS R01 HD084563NIDCD NIH HHS F31 DC018219NIDCD NIH HHS R01 DC020048NIMH NIH HHS K23 MH111955
6 · The paper itself

Abstract

purposeCommunication complexity and communicative function are important features of prelinguistic communication that are related to later language outcomes. However, little is known about how these early prelinguistic features present in young children with neurogenetic syndromes (NGS). This study aims to characterize prelinguistic complexity and function of children with three NGS: Angelman syndrome (AS), Down syndrome (DS) and fragile X syndrome (FXS).

methodSeventy-two infants aged 5-31 months (16 AS, 24 DS, 13 FXS, 19 low-risk control [LRC] infants) completed a parent-child interaction from which their prelinguistic communication was coded using the Communication Complexity Scale. Communication complexity (degree to which eye gaze, gestures, and vocalizations are integrated) and function (communication for the purposes of joint attention or behavior regulation) were compared among groups.

resultsThe DS group used the most complex communication of the syndrome groups and in many ways demonstrated similar profiles to the LRC group. The AS and FXS groups exhibited the lowest overall communication complexity when covarying age, but their levels of complexity were similar to those of the LRC group when accounting for developmental level. The DS group showed a relative strength in communication for the purposes of behavior regulation. The FXS group demonstrated the lowest likelihood of using communication for the purposes of joint attention, while the AS group exhibited the lowest likelihood of communicating for the purposes of behavior regulation.

conclusionsChildren with NGS exhibit nuanced differences in prelinguistic communication profiles that indicate unique strengths and areas of need. Additional work is needed to disentangle the effects of age and developmental level on prelinguistic communication profiles and to explore how these profiles are related to later language outcomes. Continuing to explore cross-group differences in prelinguistic communication may facilitate more targeted intervention and sensitive phenotyping among children with rare NGS.

Indexed as

Angelman SyndromeChild LanguageCommunicationDown SyndromeFragile X SyndromeChild, PreschoolFemaleGesturesHumansInfantMaleParent-Child Relations

Identifiers

PMID40664354
PMCPMC12384940

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.