Literature DB >> 20966389

Prevalence and phenotype of childhood apraxia of speech in youth with galactosemia.

Lawrence D Shriberg1, Nancy L Potter, Edythe A Strand.   

Abstract

PURPOSE: In this article, the authors address the hypothesis that the severe and persistent speech disorder reported in persons with galactosemia meets contemporary diagnostic criteria for childhood apraxia of speech (CAS). A positive finding for CAS in this rare metabolic disorder has the potential to impact treatment of persons with galactosemia and inform explanatory perspectives on CAS in neurological, neurodevelopmental, and idiopathic contexts.
METHOD: Thirty-three youth with galactosemia and significant prior or persistent speech sound disorder were assessed in their homes in 17 states. Participants completed a protocol yielding information on their cognitive, structural, sensorimotor, language, speech, prosody, and voice status and function.
RESULTS: Eight of the 33 participants (24%) met contemporary diagnostic criteria for CAS. Two participants, 1 of whom was among the 8 with CAS, met criteria for ataxic or hyperkinetic dysarthria. Groupwise findings for the remaining 24 participants are consistent with a classification category termed Motor Speech Disorder-Not Otherwise Specified (Shriberg, Fourakis et al., 2010a).
CONCLUSION: The authors estimate the prevalence of CAS in galactosemia at 18 per hundred-180 times the estimated risk for idiopathic CAS. Findings support the need to study risk factors for the high occurrence of motor speech disorders in galactosemia despite early compliant dietary management.

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Mesh:

Year:  2010        PMID: 20966389      PMCID: PMC3070858          DOI: 10.1044/1092-4388(2010/10-0068)

Source DB:  PubMed          Journal:  J Speech Lang Hear Res        ISSN: 1092-4388            Impact factor:   2.297


  42 in total

1.  Developmental apraxia of speech: I. Descriptive and theoretical perspectives.

Authors:  L D Shriberg; D M Aram; J Kwiatkowski
Journal:  J Speech Lang Hear Res       Date:  1997-04       Impact factor: 2.297

2.  Neuropsychological and linguistic follow-up studies of children with galactosaemia from an unscreened population.

Authors:  T W Hansen; B Henrichsen; R K Rasmussen; A Carling; A B Andressen; O Skjeldal
Journal:  Acta Paediatr       Date:  1996-10       Impact factor: 2.299

3.  Unusual late neurological sequelae in galactosaemia.

Authors:  J E Jan; R A Wilson
Journal:  Dev Med Child Neurol       Date:  1973-02       Impact factor: 5.449

4.  Perceptual and acoustic reliability estimates for the Speech Disorders Classification System (SDCS).

Authors:  Lawrence D Shriberg; Marios Fourakis; Sheryl D Hall; Heather B Karlsson; Heather L Lohmeier; Jane L McSweeny; Nancy L Potter; Alison R Scheer-Cohen; Edythe A Strand; Christie M Tilkens; David L Wilson
Journal:  Clin Linguist Phon       Date:  2010-10       Impact factor: 1.346

5.  Verbal dyspraxia and galactosemia.

Authors:  Amy Leigh Webb; Rani H Singh; Mary Jane Kennedy; Louis J Elsas
Journal:  Pediatr Res       Date:  2003-03       Impact factor: 3.756

6.  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

7.  A diagnostic marker for childhood apraxia of speech: the lexical stress ratio.

Authors:  Lawrence D Shriberg; Thomas F Campbell; Heather B Karlsson; Roger L Brown; Jane L McSweeny; Connie J Nadler
Journal:  Clin Linguist Phon       Date:  2003 Oct-Nov       Impact factor: 1.346

8.  A diagnostic marker for childhood apraxia of speech: the coefficient of variation ratio.

Authors:  Lawrence D Shriberg; Jordan R Green; Thomas F Campbell; Jane L McSweeny; Alison R Scheer
Journal:  Clin Linguist Phon       Date:  2003 Oct-Nov       Impact factor: 1.346

9.  A molecular approach to galactosemia.

Authors:  L J Elsas; S Langley; E M Paulk; L N Hjelm; P P Dembure
Journal:  Eur J Pediatr       Date:  1995       Impact factor: 3.183

10.  Outcomes analysis of verbal dyspraxia in classic galactosemia.

Authors:  A Robertson; R H Singh; N V Guerrero; M Hundley; L J Elsas
Journal:  Genet Med       Date:  2000 Mar-Apr       Impact factor: 8.822

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  48 in total

1.  Language Skill Mediates the Relationship Between Language Load and Articulatory Variability in Children With Language and Speech Sound Disorders.

Authors:  Janet Vuolo; Lisa Goffman
Journal:  J Speech Lang Hear Res       Date:  2018-12-10       Impact factor: 2.297

2.  The hypothesis of apraxia of speech in children with autism spectrum disorder.

Authors:  Lawrence D Shriberg; Rhea Paul; Lois M Black; Jan P van Santen
Journal:  J Autism Dev Disord       Date:  2011-04

3.  Tongue Strength in Children With and Without Speech Sound Disorders.

Authors:  Nancy L Potter; Yves Nievergelt; Mark VanDam
Journal:  Am J Speech Lang Pathol       Date:  2019-02-28       Impact factor: 2.408

Review 4.  A Diagnostic Marker to Discriminate Childhood Apraxia of Speech From Speech Delay: I. Development and Description of the Pause Marker.

Authors:  Lawrence D Shriberg; Edythe A Strand; Marios Fourakis; Kathy J Jakielski; Sheryl D Hall; Heather B Karlsson; Heather L Mabie; Jane L McSweeny; Christie M Tilkens; David L Wilson
Journal:  J Speech Lang Hear Res       Date:  2017-04-14       Impact factor: 2.297

Review 5.  Appropriateness of newborn screening for classic galactosaemia: a systematic review.

Authors:  L Varela-Lema; L Paz-Valinas; G Atienza-Merino; R Zubizarreta-Alberdi; R Vizoso Villares; M López-García
Journal:  J Inherit Metab Dis       Date:  2016-04-26       Impact factor: 4.982

6.  Phenotype of FOXP2 haploinsufficiency in a mother and son.

Authors:  Gregory M Rice; Gordana Raca; Kathy J Jakielski; Jennifer J Laffin; Christina M Iyama-Kurtycz; Sigan L Hartley; Rae E Sprague; Anne T Heintzelman; Lawrence D Shriberg
Journal:  Am J Med Genet A       Date:  2011-11-21       Impact factor: 2.802

7.  Childhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndrome.

Authors:  Gordana Raca; Becky S Baas; Salman Kirmani; Jennifer J Laffin; Craig A Jackson; Edythe A Strand; Kathy J Jakielski; Lawrence D Shriberg
Journal:  Eur J Hum Genet       Date:  2012-08-22       Impact factor: 4.246

8.  Cryptic residual GALT activity is a potential modifier of scholastic outcome in school age children with classic galactosemia.

Authors:  Emily L Ryan; Mary Ellen Lynch; Elles Taddeo; Tyler J Gleason; Michael P Epstein; Judith L Fridovich-Keil
Journal:  J Inherit Metab Dis       Date:  2013-01-15       Impact factor: 4.982

9.  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

10.  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

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