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Research Article
Research Article
June 2006

Speech, Prosody, and Voice Characteristics of a Mother and Daughter With a 7;13 Translocation Affecting FOXP2

Publication: Journal of Speech, Language, and Hearing Research
Volume 49, Number 3
Pages 500-525

Abstract

Purpose

The primary goal of this case study was to describe the speech, prosody, and voice characteristics of a mother and daughter with a breakpoint in a balanced 7;13 chromosomal translocation that disrupted the transcription gene, FOXP2 (cf. J. B. Tomblin et al., 2005). As with affected members of the widely cited KE family, whose communicative disorders have been associated with a point mutation in the FOXP2 gene, both mother and daughter had cognitive, language, and speech challenges. A 2nd goal of the study was to illustrate in detail, the types of speech, prosody, and voice metrics that can contribute to phenotype sharpening in speech-genetics research.

Method

A speech, prosody, and voice assessment protocol was administered twice within a 4-month period. Analyses were aided by comparing profiles from the present speakers (the TB family) with those from 2 groups of adult speakers: 7 speakers with acquired (with one exception) spastic or spastic-flaccid dysarthria and 14 speakers with acquired apraxia of speech.

Results

The descriptive and inferential statistical findings for 13 speech, prosody, and voice variable supported the conclusion that both mother and daughter had spastic dysarthria, an apraxia of speech, and residual developmental distortion errors.

Conclusion

These findings are consistent with, but also extend, the reported communicative disorders in affected members of the KE family. A companion article (K. J. Ballard, L. D. Shriberg, J. R. Duffy, & J. B. Tomblin, 2006) reports information from the orofacial and speech motor control measures administered to the same family; reports on neuropsychological and neuroimaging findings are in preparation.

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Information & Authors

Information

Published In

Journal of Speech, Language, and Hearing Research
Volume 49Number 3June 2006
Pages: 500-525

History

  • Received: Mar 24, 2005
  • Revised: Jul 13, 2005
  • Accepted: Oct 13, 2005
  • Published in issue: Jun 1, 2006

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Key Words

  1. apraxia
  2. articulation
  3. dysarthria
  4. genetics
  5. phonology

Authors

Affiliations

Lawrence D. Shriberg [email protected]
University of Wisconsin—Madison
Kirrie J. Ballard
J. Bruce Tomblin
Joseph R. Duffy
Katharine H. Odell
Charles A. Williams
University of Florida, Gainesville

Notes

Contact author: Lawrence D. Shriberg, Room 439, Waisman Research Center, University of Wisconsin—Madison, 1500 Highland Avenue, Madison, WI 53705. Email: [email protected]

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