Literature DB >> 25755104

Speech and language in a genotyped cohort of individuals with Kabuki syndrome.

Angela T Morgan1,2,3, Cristina Mei1,2, Annette Da Costa1,2,3, Joanne Fifer1, Damien Lederer4, Valérie Benoit4, Margaret J McMillin5, Kati J Buckingham5, Michael J Bamshad5,6, Kate Pope7, Susan M White2,3,7.   

Abstract

Speech and language deficits are commonly associated with Kabuki syndrome. Yet little is known regarding the specific symptomatology of these disorders, preventing use of targeted treatment programs. Here we detail speech and language in 16 individuals with Kabuki syndrome (thirteen with KMT2D mutations, one with a KDM6A mutation, and two mutation-negative cases), aged 4-21 years. The most striking speech deficit was dysarthria, characterised by imprecise consonants, harsh vocal quality, hypernasality, reduced rate and stress, and distorted pitch. Oromotor functioning was also impaired. Delayed, rather than disordered, articulation and phonology was common. Both receptive and expressive language abilities were reduced in the majority and deficits were noted across all language sub-domains (i.e., semantics, syntax, morphology, and pragmatics) with no clear differentiation or specific language profile. Individuals with Kabuki syndrome present with a heterogenous pattern of oromotor, speech, and language deficits. This variability fits with the multisystem nature of the disorder, which may encompass neurological, orofacial structural, hearing, and cognitive deficits, any or all of which may contribute to speech or language impairment. Our results suggest that all individuals with Kabuki syndrome have some level of communication deficit, warranting speech pathology involvement in all cases.
© 2015 Wiley Periodicals, Inc.

Entities:  

Keywords:  Kabuki syndrome; dysarthria; language; oromotor; speech

Mesh:

Year:  2015        PMID: 25755104     DOI: 10.1002/ajmg.a.37026

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  11 in total

Review 1.  Decoding the biology of language and its implications in language acquisition.

Authors:  D R Rahul; R Joseph Ponniah
Journal:  J Biosci       Date:  2019-03       Impact factor: 1.826

2.  Early speech development in Koolen de Vries syndrome limited by oral praxis and hypotonia.

Authors:  Angela T Morgan; Leenke van Haaften; Karen van Hulst; Carol Edley; Cristina Mei; Tiong Yang Tan; David Amor; Simon E Fisher; David A Koolen
Journal:  Eur J Hum Genet       Date:  2017-12-11       Impact factor: 4.246

3.  Deep phenotyping of speech and language skills in individuals with 16p11.2 deletion.

Authors:  Cristina Mei; Evelina Fedorenko; David J Amor; Amber Boys; Caitlyn Hoeflin; Peter Carew; Trent Burgess; Simon E Fisher; Angela T Morgan
Journal:  Eur J Hum Genet       Date:  2018-02-14       Impact factor: 4.246

4.  A comparative analysis of KMT2D missense variants in Kabuki syndrome, cancers and the general population.

Authors:  Víctor Faundes; Geraldine Malone; William G Newman; Siddharth Banka
Journal:  J Hum Genet       Date:  2018-11-20       Impact factor: 3.172

Review 5.  Kabuki syndrome: review of the clinical features, diagnosis and epigenetic mechanisms.

Authors:  Yi-Rou Wang; Nai-Xin Xu; Jian Wang; Xiu-Min Wang
Journal:  World J Pediatr       Date:  2019-10-05       Impact factor: 2.764

6.  Near complete deletion of KMT2D in a college student.

Authors:  Catherine Gooch; Jaclyn Paige Souder; Matthew L Tedder; Jennifer Kerkhof; Jennifer A Lee; Raymond J Louie; Bekim Sadikovic; Robin S Fletcher; Nathaniel H Robin
Journal:  Am J Med Genet A       Date:  2022-01-18       Impact factor: 2.802

7.  Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment.

Authors:  Xiaowei Sylvia Chen; Rose H Reader; Alexander Hoischen; Joris A Veltman; Nuala H Simpson; Clyde Francks; Dianne F Newbury; Simon E Fisher
Journal:  Sci Rep       Date:  2017-04-25       Impact factor: 4.379

8.  Neurobehavioral features in individuals with Kabuki syndrome.

Authors:  Cristina Caciolo; Paolo Alfieri; Giorgia Piccini; Maria Cristina Digilio; Francesca Romana Lepri; Marco Tartaglia; Deny Menghini; Stefano Vicari
Journal:  Mol Genet Genomic Med       Date:  2018-03-13       Impact factor: 2.183

9.  Longitudinal Cognitive and Behavioral Presentation of Adult Female with Kabuki Syndrome.

Authors:  Pamela Ventola; Anamiguel Pomales-Ramos; Elizabeth A DeLucia
Journal:  Am J Case Rep       Date:  2019-04-02

10.  A novel KMT2D mutation resulting in Kabuki syndrome: A case report.

Authors:  Jun Lu; Guiling Mo; Yaojun Ling; Lijuan Ji
Journal:  Mol Med Rep       Date:  2016-08-26       Impact factor: 2.952

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