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

American Journal of Medical Genetics. Part a
Angela T MorganSusan M White

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 impairm...Continue Reading

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Citations

Mar 15, 2018·Molecular Genetics & Genomic Medicine·Cristina CacioloStefano Vicari
Feb 16, 2018·European Journal of Human Genetics : EJHG·Cristina MeiAngela T Morgan
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Dec 12, 2017·European Journal of Human Genetics : EJHG·Angela T MorganDavid A Koolen
Jun 27, 2020·Developmental Medicine and Child Neurology·Cristina MeiAngela T Morgan
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