Speech, Language, Hearing, and Otopathology Results From the International Smith--Magenis Syndrome Patient Registry.

Purpose: Smith--Magenis syndrome (SMS), a rare, genetically linked complex developmental disorder caused by a deletion or mutation within chromosome 17p11.2, is associated with delays in speech-language development, otopathology, and hearing loss, yet previous studies lack comprehensive descriptions...

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Bibliographic Details
Published in:	Journal of Speech, Language & Hearing Research Vol. 67; no. 3; pp. 917 - 939
Main Authors:	Brennan, Christine, Smith, Mara Louise, Baiduc, Rachael R., O'Connor, Liam
Format:	Article
Published:	American Speech-Language-Hearing Association Mar2024
Subjects:	Language disorders Communication Speech disorders Otitis media Pearson correlation (Statistics) Questionnaires Smith-Magenis syndrome Reporting of diseases Descriptive statistics Chi-squared test Acquisition of data Inferential statistics Middle ear ventilation Hearing disorders Text messages Human voice Disease complications
Online Access:	View this record in EBSCOhost