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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Detalles Bibliográficos
Publicado en:	Journal of Speech, Language & Hearing Research Vol. 67; no. 3; pp. 917 - 939
Autores principales:	Brennan, Christine, Smith, Mara Louise, Baiduc, Rachael R., O'Connor, Liam
Formato:	Artículo
Publicado:	American Speech-Language-Hearing Association Mar2024
Materias:	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
Acceso en línea:	Ver este registro en EBSCOhost

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