FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W4309314545> ?p ?o ?g. }

• W4309314545 abstract "Williams syndrome is a neurodevelopmental genetic disorder characterized by a unique phenotype, including mild to moderate intellectual disability and an uneven neuropsychological profile of relative strengths and weaknesses. Language structure components (i.e., phonology, morphosyntax, and vocabulary) have been considered an area of specific ability compared to pragmatic language use. However, research on phonological development in Williams syndrome is very scarce, and it suggests atypical patterns. Therefore, the aim of the present study was to explore the profiles of late phonological development in Spanish-speaking children, adolescents, and adults with Williams syndrome, based on the analysis of five classes of processes (Syllable Structure, Substitution, Omission, Assimilation, and Addition) in spontaneous speech. The phonological profiles of seven children (aged 3-8 years), and seven adolescents and young adults (aged 14-25 years) with Williams syndrome were compared with two normative groups of typically developing (TD) children at different stages of late phonological development (aged 3 and 5 years). The frequency of phonological processes in the group of children with Williams syndrome was similar to that of 3-year-old TD children, which suggests that they would be in the first stage of late phonological development (expansion stage). The group of older individuals with Williams syndrome showed a much lower frequency of processes, similar to that of 5-year-old TD children in the last stage of phonological development (resolution stage). However, their phonological processes appeared to be persistent and independent of chronological age. Furthermore, asynchronies in quantitative and qualitative profiles (relative frequency) indicated atypical and complex trajectories in late phonological development, which cannot be described as simply delayed or protracted. Remarkable individual differences were observed, especially in the group of adolescents and adults with Williams syndrome, although the majority of cases conformed to the modal profiles of their groups. A major tendency for Omission, including final consonant deletion, may be considered atypical and specific to Williams syndrome at all ages. The results of the present study raise the need for continued and appropriate phonological assessment and treatment for people with Williams syndrome across the lifespan." @default.
• W4309314545 created "2022-11-26" @default.
• W4309314545 creator A5029536208 @default.
• W4309314545 creator A5044742434 @default.
• W4309314545 creator A5076234258 @default.
• W4309314545 date "2022-11-16" @default.
• W4309314545 modified "2023-10-01" @default.
• W4309314545 title "Late phonological development in Williams syndrome" @default.
• W4309314545 cites W1684631486 @default.
• W4309314545 cites W1954770225 @default.
• W4309314545 cites W1964380283 @default.
• W4309314545 cites W1970445122 @default.
• W4309314545 cites W1971431159 @default.
• W4309314545 cites W1972909055 @default.
• W4309314545 cites W1973589300 @default.
• W4309314545 cites W1975418600 @default.
• W4309314545 cites W1978359781 @default.
• W4309314545 cites W1990359376 @default.
• W4309314545 cites W2003159758 @default.
• W4309314545 cites W2003875845 @default.
• W4309314545 cites W2007857174 @default.
• W4309314545 cites W2009023961 @default.
• W4309314545 cites W2010972204 @default.
• W4309314545 cites W2016248942 @default.
• W4309314545 cites W2016568406 @default.
• W4309314545 cites W2023149246 @default.
• W4309314545 cites W2027577066 @default.
• W4309314545 cites W2034508290 @default.
• W4309314545 cites W2035202753 @default.
• W4309314545 cites W2039167130 @default.
• W4309314545 cites W2039730733 @default.
• W4309314545 cites W2042675530 @default.
• W4309314545 cites W2055848870 @default.
• W4309314545 cites W2057728436 @default.
• W4309314545 cites W2071542196 @default.
• W4309314545 cites W2082125793 @default.
• W4309314545 cites W2093739837 @default.
• W4309314545 cites W2097106481 @default.
• W4309314545 cites W2101698702 @default.
• W4309314545 cites W2107148628 @default.
• W4309314545 cites W2108409919 @default.
• W4309314545 cites W2111312122 @default.
• W4309314545 cites W2112615525 @default.
• W4309314545 cites W2127771914 @default.
• W4309314545 cites W2128118091 @default.
• W4309314545 cites W2135232648 @default.
• W4309314545 cites W2139009087 @default.
• W4309314545 cites W2140992043 @default.
• W4309314545 cites W2141775198 @default.
• W4309314545 cites W2142578090 @default.
• W4309314545 cites W2145146029 @default.
• W4309314545 cites W2156076108 @default.
• W4309314545 cites W2161886243 @default.
• W4309314545 cites W2162039637 @default.
• W4309314545 cites W2166051244 @default.
• W4309314545 cites W2343825523 @default.
• W4309314545 cites W2490324385 @default.
• W4309314545 cites W2512883586 @default.
• W4309314545 cites W2513929929 @default.
• W4309314545 cites W2593803248 @default.
• W4309314545 cites W2613084976 @default.
• W4309314545 cites W2625580461 @default.
• W4309314545 cites W2759329582 @default.
• W4309314545 cites W2770501375 @default.
• W4309314545 cites W2784258302 @default.
• W4309314545 cites W2889194909 @default.
• W4309314545 cites W2900910043 @default.
• W4309314545 cites W2987411828 @default.
• W4309314545 cites W2992961513 @default.
• W4309314545 cites W3010877999 @default.
• W4309314545 cites W3032015553 @default.
• W4309314545 cites W3034336040 @default.
• W4309314545 cites W3040724396 @default.
• W4309314545 cites W3108320074 @default.
• W4309314545 cites W3109388646 @default.
• W4309314545 cites W3162483211 @default.
• W4309314545 cites W3165702736 @default.
• W4309314545 cites W4211151215 @default.
• W4309314545 cites W4211199548 @default.
• W4309314545 cites W4211265573 @default.
• W4309314545 cites W4220999665 @default.
• W4309314545 cites W4244459743 @default.
• W4309314545 cites W4251661431 @default.
• W4309314545 cites W4253144361 @default.
• W4309314545 cites W4255642126 @default.
• W4309314545 doi "https://doi.org/10.3389/fpsyg.2022.992512" @default.
• W4309314545 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/36467192" @default.
• W4309314545 hasPublicationYear "2022" @default.
• W4309314545 type Work @default.
• W4309314545 citedByCount "0" @default.
• W4309314545 crossrefType "journal-article" @default.
• W4309314545 hasAuthorship W4309314545A5029536208 @default.
• W4309314545 hasAuthorship W4309314545A5044742434 @default.
• W4309314545 hasAuthorship W4309314545A5076234258 @default.
• W4309314545 hasBestOaLocation W43093145451 @default.
• W4309314545 hasConcept C109089402 @default.
• W4309314545 hasConcept C111472728 @default.
• W4309314545 hasConcept C118552586 @default.
• W4309314545 hasConcept C138496976 @default.
• W4309314545 hasConcept C138885662 @default.

• next