Document Type

Article

Abstract

People with Phelan–McDermid syndrome (PMS) have reduced speech and language abilities, yet little research has profiled the communication abilities in this population. The purpose of this study was threefold: identifying the language and communication profiles of school-aged children with PMS, identifying genetic contributions to language and communication abilities, and determining the feasibility of remote data collection for research purposes. A speech language pathologist used standardized assessments and direct evaluations by video conferencing to evaluate language and communication abilities. Sixteen children and adolescents were evaluated: 5 with SHANK3 pathogenic variants, 9 with 22q13 deletions including SHANK3 (PMS-SHANK3 related), and 2 with 22q13 deletions preserving SHANK3 (PMS-SHANK3 unrelated). All showed moderate-to-severe language impairment across all assessments. Females demonstrated higher communication abilities than males. Haploinsufficiency of SHANK3 appears to be the main driver of language impairment in PMS; however, participants with preserved SHANK3 also scored in the impairment range, suggesting other contributions from 22q13 genes to the language phenotype. This study demonstrates the efficacy of using standardized instruments and remote data collection methods to assess communication in PMS. Remote methods may be helpful for the assessment of other genetic disorders involving language phenotypes.

Digital Object Identifier (DOI)

https://doi.org/10.1002/ajmg.a.70117

Rights

© 2026 The Author(s). American Journal of Medical Genetics Part A published by Wiley Periodicals LLC.

This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.

APA Citation

Quadri‐Valverde, S., Klusek, J., Ward, L. D., Ivankovic, D., Powers, N., Shankar, V., Lyman, R. A., Mackay, T. F. C., Bridges, W., Phelan, K., Rogers, C., Boccuto, L., & Sarasua, S. M. (2026). Remote Language Assessment in School‐Age Children With Phelan– McDermid Syndrome and Genotype–Phenotype Correlation. American Journal of Medical Genetics Part A.https://doi.org/10.1002/ajmg.a.70117

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