Literature DB >> 21909176

A multigenerational family study of oral and hand motor sequencing ability provides evidence for a familial speech sound disorder subtype.

Beate Peter1, Wendy H Raskind.   

Abstract

PURPOSE: To evaluate phenotypic expressions of speech sound disorder (SSD) in multigenerational families with evidence of familial forms of SSD.
METHOD: Members of five multigenerational families (N = 36) produced rapid sequences of monosyllables and disyllables and tapped computer keys with repetitive and alternating movements.
RESULTS: Measures of repetitive and alternating motor speed were correlated within and between the two motor systems. Repetitive and alternating motor speeds increased in children and decreased in adults as a function of age. In two families with children who had severe speech deficits consistent with disrupted praxis, slowed alternating, but not repetitive, oral movements characterized most of the affected children and adults with a history of SSD, and slowed alternating hand movements were seen in some of the biologically related participants as well.
CONCLUSION: Results are consistent with a familial motor-based SSD subtype with incomplete penetrance, motivating new clinical questions about motor-based intervention not only in the oral but also the limb system.

Entities:  

Year:  2011        PMID: 21909176      PMCID: PMC3169648          DOI: 10.1097/TLD.0b013e318217b855

Source DB:  PubMed          Journal:  Top Lang Disord        ISSN: 0271-8294


  36 in total

1.  Prevalence of speech delay in 6-year-old children and comorbidity with language impairment.

Authors:  L D Shriberg; J B Tomblin; J L McSweeny
Journal:  J Speech Lang Hear Res       Date:  1999-12       Impact factor: 2.297

2.  Reliability and validity of a computerized neurocognitive test battery, CNS Vital Signs.

Authors:  C Thomas Gualtieri; Lynda G Johnson
Journal:  Arch Clin Neuropsychol       Date:  2006-10-02       Impact factor: 2.813

Review 3.  Neuropsychology and genetics of speech, language, and literacy disorders.

Authors:  Robin L Peterson; Lauren M McGrath; Shelley D Smith; Bruce F Pennington
Journal:  Pediatr Clin North Am       Date:  2007-06       Impact factor: 3.278

4.  Localisation of a gene implicated in a severe speech and language disorder.

Authors:  S E Fisher; F Vargha-Khadem; K E Watkins; A P Monaco; M E Pembrey
Journal:  Nat Genet       Date:  1998-02       Impact factor: 38.330

5.  The prevalence of stuttering, voice, and speech-sound disorders in primary school students in Australia.

Authors:  David H McKinnon; Sharynne McLeod; Sheena Reilly
Journal:  Lang Speech Hear Serv Sch       Date:  2007-01       Impact factor: 2.983

6.  Clinical assessment of oropharyngeal motor development in young children.

Authors:  J Robbins; T Klee
Journal:  J Speech Hear Disord       Date:  1987-08

7.  Risk factors for speech delay of unknown origin in 3-year-old children.

Authors:  Thomas F Campbell; Christine A Dollaghan; Howard E Rockette; Jack L Paradise; Heidi M Feldman; Lawrence D Shriberg; Diane L Sabo; Marcia Kurs-Lasky
Journal:  Child Dev       Date:  2003 Mar-Apr

8.  A forkhead-domain gene is mutated in a severe speech and language disorder.

Authors:  C S Lai; S E Fisher; J A Hurst; F Vargha-Khadem; A P Monaco
Journal:  Nature       Date:  2001-10-04       Impact factor: 49.962

Review 9.  Hearing loss: mechanisms revealed by genetics and cell biology.

Authors:  Amiel A Dror; Karen B Avraham
Journal:  Annu Rev Genet       Date:  2009       Impact factor: 16.830

10.  Speech and language skills of parents of children with speech sound disorders.

Authors:  Barbara A Lewis; Lisa A Freebairn; Amy J Hansen; Lara Miscimarra; Sudha K Iyengar; H Gerry Taylor
Journal:  Am J Speech Lang Pathol       Date:  2007-05       Impact factor: 2.408

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  8 in total

1.  Direct and octave-shifted pitch matching during nonword imitations in men, women, and children.

Authors:  Beate Peter; Bronsyn Foster; Heather Haas; Kyle Middleton; Kiersten McKibben
Journal:  J Voice       Date:  2014-11-25       Impact factor: 2.009

2.  Sequential processing deficit as a shared persisting biomarker in dyslexia and childhood apraxia of speech.

Authors:  Beate Peter; Hope Lancaster; Caitlin Vose; Kyle Middleton; Carol Stoel-Gammon
Journal:  Clin Linguist Phon       Date:  2017-09-21       Impact factor: 1.346

3.  Motor sequencing deficit as an endophenotype of speech sound disorder: a genome-wide linkage analysis in a multigenerational family.

Authors:  Beate Peter; Mark Matsushita; Wendy H Raskind
Journal:  Psychiatr Genet       Date:  2012-10       Impact factor: 2.458

4.  Associations among measures of sequential processing in motor and linguistics tasks in adults with and without a family history of childhood apraxia of speech: a replication study.

Authors:  Le Button; Beate Peter; Carol Stoel-Gammon; Wendy H Raskind
Journal:  Clin Linguist Phon       Date:  2013-01-22       Impact factor: 1.346

5.  Deficits in sequential processing manifest in motor and linguistic tasks in a multigenerational family with childhood apraxia of speech.

Authors:  Beate Peter; Le Button; Carol Stoel-Gammon; Kathy Chapman; Wendy H Raskind
Journal:  Clin Linguist Phon       Date:  2013-01-22       Impact factor: 1.346

6.  Cognitive, Linguistic, and Motor Abilities in a Multigenerational Family with Childhood Apraxia of Speech.

Authors:  Bronwyn Carrigg; Louise Parry; Elise Baker; Lawrence D Shriberg; Kirrie J Ballard
Journal:  Arch Clin Neuropsychol       Date:  2016-12-01       Impact factor: 2.813

7.  Differences and Commonalities in Children with Childhood Apraxia of Speech and Comorbid Neurodevelopmental Disorders: A Multidimensional Perspective.

Authors:  Anna Maria Chilosi; Irina Podda; Ivana Ricca; Alessandro Comparini; Beatrice Franchi; Simona Fiori; Rosa Pasquariello; Claudia Casalini; Paola Cipriani; Filippo Maria Santorelli
Journal:  J Pers Med       Date:  2022-02-19

8.  Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech.

Authors:  Beate Peter; Ellen M Wijsman; Alejandro Q Nato; Mark M Matsushita; Kathy L Chapman; Ian B Stanaway; John Wolff; Kaori Oda; Virginia B Gabo; Wendy H Raskind
Journal:  PLoS One       Date:  2016-04-27       Impact factor: 3.240

  8 in total

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