Articulation in Beckwith-Wiedemann Syndrome: Two Case Studies

Author:

Borsel John Van1,Morlion Bieke1,Snick Kathleen Van1,Leroy Jules S.2

Affiliation:

1. UZ Gent, Centrum voor Gehoor- en Spraakrevalidatie, Gent, Belgium

2. UZ Gent, Pediatrie, Gent, Belgium

Abstract

Beckwith-Wiedemann syndrome (BWS) is a genetic disorder with abdominal wall defects, gigantism, and macroglossia as its main characteristics. A number of investigators have reported the presence of articulation errors in individuals with BWS due to macroglossia. However, few data are available on the exact nature of the articulation problems of subjects with BWS. This paper presents two case studies that highlight the articulatory characteristics associated with BWS. Subjects were a boy aged 5 years 9 months and a girl aged 3 years 6 months. A phonetic analysis was conducted in which it was found that primarily consonants with an anterior place of articulation were affected. The error patterns appeared to be related to inappropriate tongue and lip postures. An observer experiment in which naive and expert observers rated speech samples from three modes of presentation (auditory-only, visual-only, and audiovisual) showed that the subjects’ speech was more disturbed visually than auditorily.

Publisher

American Speech Language Hearing Association

Subject

Speech and Hearing,Linguistics and Language,Developmental and Educational Psychology,Otorhinolaryngology

Reference30 articles.

1. The influence of genetic syndromes upon oral communication skills;Adler S.;Journal of Speech and Hearing Disorders,1976

2. Beckwith J. B. (1963 November). Extreme cytomegaly of the fetal adrenal cortex omphalocele hyperplasia of kidneys and pancreas and leydigcell hyperplasia: Another syndrome? Paper presented at the Annual Meeting of the Western Society for Pediatric Research Los Angeles CA.

3. Clinical features and natural history of Beckwith-Wiedemann syndrome: Presentation of 74 new cases;Elliott M.;Clinical Genetics,1994

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