Characterization of speech and language phenotype in the 8p23.1 syndrome
- PMID: 38671247
- PMCID: PMC11564291
- DOI: 10.1007/s00787-024-02448-0
Characterization of speech and language phenotype in the 8p23.1 syndrome
Abstract
The 8p23.1 duplication syndrome is a rare genetic condition with an estimated prevalence rate of 1 out of 58,000. Although the syndrome was associated with speech and language delays, a comprehensive assessment of speech and language functions has not been undertaken in this population. To address this issue, the present study reports rigorous speech and language, in addition to oral-facial and developmental, assessment of a 50-month-old Turkish-speaking boy who was diagnosed with the 8p23.1 duplication syndrome. Standardized tests of development, articulation and phonology, receptive and expressive language and a language sample analysis were administered to characterize speech and language skills in the patient. The language sample was obtained in an ecologically valid, free play and conversation context. The language sample was then analyzed and compared to a database of age-matched typically-developing children (n = 33) in terms of intelligibility, morphosyntax, semantics/vocabulary, discourse, verbal facility and percentage of errors at word and utterance levels. The results revealed mild to severe problems in articulation and phonology, receptive and expressive language skills, and morphosyntax (mean length of utterance in morphemes). Future research with larger sample sizes and employing detailed speech and language assessment is needed to delineate the speech and language profile in individuals with the 8p23.1 duplication syndrome, which will guide targeted speech and language interventions.
Keywords: 8p23.1 duplication syndrome; Language; Speech.
© 2024. The Author(s).
Conflict of interest statement
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References
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- Barber JCK, Rosenfeld JA, Foulds N et al (2013) 8P23.1 duplication syndrome; Common, confirmed, and Novel features in six further patients. Am J Med Genet Part A 161:487–500. 10.1002/ajmg.a.35767 - PubMed
-
- Nusbaum C, Mikkelsen TS, Zody MC et al (2006) DNA sequence and analysis of human chromosome 8. Nature 439:331–335. 10.1038/nature04406 - PubMed
-
- Barber JCK, Maloney V, Hollox EJ et al (2005) Duplications and copy number variants of 8p23.1 are cytogenetically indistinguishable but distinct at the molecular level. Eur J Hum Genet 13:1131–1136. 10.1038/sj.ejhg.5201475 - PubMed
-
- Barber JCK, Rosenfeld JA, Graham JM et al (2015) Inside the 8p23.1 duplication syndrome; eight microduplications of likely or uncertain clinical significance. Am J Med Genet Part A 167:2052–2064. 10.1002/ajmg.a.37120 - PubMed
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