International Journal of Speech and Audiology
2023, Vol. 4, Issue 1, Part A
Speech and language profile of Apert syndrome: A single case report
Author(s): V Monish, S Powlin Arockia Catherine and MK Rajasekar
Abstract: Introduction: Apert syndrome is a rare congenital condition with a midface hypoplasia, symmetric syndactyly of the hands and feet, and autosomal dominant inheritance. Individuals with Apert syndrome had a high prevalence of language disorders, speech sound disorders and hearing problems. Aim: The aim of the study was to document the speech and language profile of a client with a diagnosis of Apert syndrome. Method: A detailed speech and language assessment was done for the client using informal and formal methods of evaluation. Results and Discussion: The client was diagnosed to have expressive language disorder with speech sound disorder secondary to Apert syndrome. The most frequent and consistent articulatory error was substitution of lingua-dental sounds for lingua alveolar and lingua palatal sounds. Conclusion: The present study would help students and professionals understand the speech and language profile of a client with Apert syndrome and assist in the assessment procedures to be followed and additionally contribute to rehabilitation strategies.
Pages: 26-28 | Views: 539 | Downloads: 347
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How to cite this article:
V Monish, S Powlin Arockia Catherine and MK Rajasekar. Speech and language profile of Apert syndrome: A single case report. International Journal of Speech and Audiology. 2023; 4(1): 26-28.
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