Individuals with Down Syndrome

A special issue of Brain Sciences (ISSN 2076-3425). This special issue belongs to the section "Neurodegenerative Diseases".

Deadline for manuscript submissions: closed (31 March 2021) | Viewed by 26344

Special Issue Editors


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Guest Editor
Department of General Psychology, University of Padua, Padua, Italy
Interests: spatial cognition; environment learning; navigation; spatial description; spatial abilities; wayfinding attitudes; individual differences; spatial memory; cognitive map

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Guest Editor
Department of General Psychology, University of Padova, Italy
Interests: Learning; memory; reading comprehension; individual and age differences

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Guest Editor
Department of Developmental and Socialization, University of Padova, Padova, Italy

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Guest Editor
Department of General Psychology, University of Padova, Via Venezia 8, Padova, Italy

Special Issue Information

Dear Colleagues,

Individuals with Down syndrome (DS) have long been of great interest to researchers. DS is a genetic syndrome caused by abnormalities on chromosome 21. The IQ of individuals with DS generally ranges between 25 and 70, and most of them reach the mental age (MA) of a five- to seven-year-old. Most research has examined strengths and weaknesses in their cognitive profile and related aspects, such as their ability to manage activities of daily living that ensure their autonomy. This Special Issue concerns this line of research, addressing and expanding on new theoretical and methodological approaches to analyzing the characteristics of this population. In particular, their cognitive profile needs to be better examined in terms of basic processes and higher-level cognitive abilities, and their impact on everyday activities (e.g., academic learning, navigation). This can be done by considering groups of individuals with DS and comparing them with groups of individuals with typical or atypical development. We also need to shed light on individual profiles, however, given the DS population’s variable performance in cognitive tasks, as well as looking at their different trajectories of cognitive development with across-ages or longitudinal studies within DS groups, and by comparison with TD individuals. 

Dr. Chiara Meneghetti
Prof. Dr. Barbara Carretti
Dr. Silvia Lanfranchi
Dr. Enrico Toffalini
Guest Editors

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Keywords

  • Down syndrome
  • cognitive profile
  • cognitive abilities
  • everyday activities
  • development trajectories

Published Papers (9 papers)

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Editorial

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4 pages, 188 KiB  
Editorial
Individuals with Down Syndrome: Editorial
by Silvia Lanfranchi, Chiara Meneghetti, Enrico Toffalini and Barbara Carretti
Brain Sci. 2022, 12(3), 398; https://doi.org/10.3390/brainsci12030398 - 16 Mar 2022
Cited by 2 | Viewed by 1935
Abstract
Down syndrome (DS) is the most common syndromic cause of intellectual disability, so it has long been of interest to researchers [...] Full article
(This article belongs to the Special Issue Individuals with Down Syndrome)

Research

Jump to: Editorial

17 pages, 1271 KiB  
Article
Reading for Comprehension in Individuals with Down Syndrome, Autism Spectrum Disorder and Typical Development: Similar or Different Patterns of Ability?
by Maja Roch, Kate Cain and Christopher Jarrold
Brain Sci. 2021, 11(7), 828; https://doi.org/10.3390/brainsci11070828 - 22 Jun 2021
Cited by 4 | Viewed by 2627
Abstract
Reading for meaning is one of the most important activities in school and everyday life. The simple view of reading (SVR) has been used as a framework for studies of reading comprehension in individuals with Down syndrome (DS). These tend to show difficulties [...] Read more.
Reading for meaning is one of the most important activities in school and everyday life. The simple view of reading (SVR) has been used as a framework for studies of reading comprehension in individuals with Down syndrome (DS). These tend to show difficulties in reading comprehension despite better developed reading accuracy. Reading comprehension difficulties are influenced by poor oral language. These difficulties are common in individuals with DS and autism spectrum disorder (ASD), but they have never been compared directly. Moreover, the components of reading for comprehension have rarely been investigated in these populations: a better understanding of the nature of reading comprehension difficulties may inform both theory and practice. The aim of this study was to determine whether reading comprehension in the two populations is accounted for by the same component skills and to what extent the reading profile of the two atypical groups differs from that of typically developing children (TD). Fifteen individuals with DS (mean age = 22 years 4 months, SD = 5 years 2 months), 21 with ASD (mean age = 13 years 2 months, SD = 1 year 6 months), and 42 TD children (mean age = 8 years 1 month, SD = 7 months) participated and were assessed on measures of receptive vocabulary, text reading and listening comprehension, oral language comprehension, and reading accuracy. The results showed similar levels in word reading accuracy and in receptive vocabulary in all three groups. By contrast, individuals with DS and ASD showed poorer non-word reading and reading accuracy in context than TD children. Both atypical groups showed poorer listening and reading text comprehension compared to TD children. Reading for comprehension, investigated through a homograph reading accuracy task, showed a different pattern for individuals with DS with respect to the other two groups: they were less sensitive to meaning while reading. According to the SVR, the current results confirm that the two atypical groups have similar profiles that overlap with that of poor comprehenders in which poor oral language comprehension constrains reading for comprehension. Full article
(This article belongs to the Special Issue Individuals with Down Syndrome)
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21 pages, 593 KiB  
Article
The Home Learning Environment of Primary School Children with Down Syndrome and Those with Williams Syndrome
by Erica Ranzato, Andrew Tolmie and Jo Van Herwegen
Brain Sci. 2021, 11(6), 733; https://doi.org/10.3390/brainsci11060733 - 31 May 2021
Cited by 4 | Viewed by 3347
Abstract
Background and aims: Research on typically developing (TD) populations has shown that the home learning environment plays a significant role in cognitive development and learning, but very little is known about the home learning environment of children with Down syndrome (DS) or children [...] Read more.
Background and aims: Research on typically developing (TD) populations has shown that the home learning environment plays a significant role in cognitive development and learning, but very little is known about the home learning environment of children with Down syndrome (DS) or children with Williams syndrome (WS). The present study examined and compared, for the first time, the home learning environment of children diagnosed with DS and children diagnosed with WS to investigate whether different cognitive profiles were reflected in their home literacy and number experiences. Methods and procedures: Quantitative and qualitative data were collected through a web-based survey from 58 parents and one foster parent of primary school children with DS (n = 35) and WS (n = 24) mostly based in the UK. The survey targeted the children’s general level of functioning and academic skills; type, format, and frequency of home learning activities; parents’ expectations for their child’s academic outcomes; parents’ attitudes towards literacy and mathematics; children’s interest towards mathematics; and the use of technology to support home learning activities. Outcomes and results: Our results showed that, overall, the home learning environment of children with DS and children with WS were similar but changed based on the child’s cognitive profile. Comparative analyses showed that parents of children with DS engaged more often in activities supporting counting than parents of children with WS, despite both groups reporting difficulties with this skill. Moreover, our results indicated that literacy-based activities occurred more often than mathematics-based activities and that the home numeracy environment was characterized by activities supporting different mathematical skills such as counting, arithmetic, and numeracy. Parents in both groups engaged with their child in both formal and informal literacy and mathematics-based activities, but informal activities occurred more often when supporting counting and number recognition skills. Conclusions and implications: The current study provides evidence that the home learning environment of children with DS and children with WS include different literacy- and mathematics-based activities and that the home learning environment changes on the basis of the child’s strengths and weaknesses. The findings are discussed in relation to previous studies and the impact on parental interventions. Full article
(This article belongs to the Special Issue Individuals with Down Syndrome)
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16 pages, 270 KiB  
Article
Is the Age of Developmental Milestones a Predictor for Future Development in Down Syndrome?
by Chiara Locatelli, Sara Onnivello, Francesca Antonaros, Agnese Feliciello, Sonia Filoni, Sara Rossi, Francesca Pulina, Chiara Marcolin, Renzo Vianello, Enrico Toffalini, Giuseppe Ramacieri, Anna Martelli, Giulia Procaccini, Giacomo Sperti, Maria Caracausi, Maria Chiara Pelleri, Lorenza Vitale, Gian Luca Pirazzoli, Pierluigi Strippoli, Guido Cocchi, Allison Piovesan and Silvia Lanfranchiadd Show full author list remove Hide full author list
Brain Sci. 2021, 11(5), 655; https://doi.org/10.3390/brainsci11050655 - 18 May 2021
Cited by 15 | Viewed by 4084
Abstract
Down Syndrome (DS) is the most common genetic alteration responsible for intellectual disability, which refers to deficits in both intellectual and adaptive functioning. According to this, individuals with Down Syndrome (DS) reach developmental milestones (e.g., sitting, walking, and babbling) in the same order [...] Read more.
Down Syndrome (DS) is the most common genetic alteration responsible for intellectual disability, which refers to deficits in both intellectual and adaptive functioning. According to this, individuals with Down Syndrome (DS) reach developmental milestones (e.g., sitting, walking, and babbling) in the same order as their typically developing peers, but later in life. Since developmental milestones are the first blocks on which development builds, the aims of the current study are to: (i) expand the knowledge of developmental milestone acquisition; and (ii) explore the relationship between developmental milestone acquisition and later development. For this purpose 105 children/adolescents with DS were involved in this study, divided in two groups, Preschoolers (n = 39) and School-age participants (n = 66). Information on the age of acquisition of Sitting, Walking, Babbling, and Sphincter Control was collected, together with cognitive, motor, and adaptive functioning. Sitting predicted later motor development, but, with age, it became less important in predicting motor development in everyday life. Babbling predicted later language development in older children. Finally, Sphincter Control emerged as the strongest predictor of motor, cognitive, language, and adaptive skills, with its role being more evident with increasing age. Our data suggest that the age of reaching the milestones considered in the study has an influence on successive development, a role that can be due to common neural substrates, the environment, and the developmental cascade effect. Full article
(This article belongs to the Special Issue Individuals with Down Syndrome)
15 pages, 286 KiB  
Article
Inhibitory Dimensions and Delay of Gratification: A Comparative Study on Individuals with Down Syndrome and Typically Developing Children
by Martina Fontana, Maria Carmen Usai, Sandra Pellizzoni and Maria Chiara Passolunghi
Brain Sci. 2021, 11(5), 636; https://doi.org/10.3390/brainsci11050636 - 14 May 2021
Cited by 4 | Viewed by 1995
Abstract
While previous research on inhibition in people with Down syndrome (DS) reported contradictory results, with no explicit theoretical model, on the other hand, a more homogeneous impaired profile on the delay of gratification skills emerged. The main goal of the present study was [...] Read more.
While previous research on inhibition in people with Down syndrome (DS) reported contradictory results, with no explicit theoretical model, on the other hand, a more homogeneous impaired profile on the delay of gratification skills emerged. The main goal of the present study was to investigate response inhibition, interference suppression, and delay of gratification in 51 individuals with DS matched for a measure of mental age (MA) with 71 typically developing (TD) children. Moreover, we cross-sectionally explored the strengths and weaknesses of these components in children and adolescents vs. adults with DS with the same MA. A battery of laboratory tasks tapping on inhibitory sub-components and delay of gratification was administrated. Results indicated that individuals with DS showed an overall worse performance compared to TD children on response inhibition and delay of gratification, while no differences emerged between the two samples on the interference suppression. Additionally, our results suggested that older individuals with DS outperformed the younger ones both in response inhibition and in the delay of gratification, whereas the interference suppression still remains impaired in adulthood. This study highlights the importance of evaluating inhibitory sub-components considering both MA and chronological age in order to promote more effective and evidence-based training for this population. Full article
(This article belongs to the Special Issue Individuals with Down Syndrome)
16 pages, 1981 KiB  
Article
Developmental Trajectories in Spatial Visualization and Mental Rotation in Individuals with Down Syndrome
by Elizabeth Maria Doerr, Barbara Carretti, Enrico Toffalini, Silvia Lanfranchi and Chiara Meneghetti
Brain Sci. 2021, 11(5), 610; https://doi.org/10.3390/brainsci11050610 - 10 May 2021
Cited by 6 | Viewed by 2061
Abstract
Background. The analysis of developmental trajectories of visuospatial abilities in individuals with Down Syndrome (DS) remains an unexplored field of investigation to examine in depth. The study aimed to fill such a gap by examining changes in two visuospatial abilities: spatial visualization (the [...] Read more.
Background. The analysis of developmental trajectories of visuospatial abilities in individuals with Down Syndrome (DS) remains an unexplored field of investigation to examine in depth. The study aimed to fill such a gap by examining changes in two visuospatial abilities: spatial visualization (the ability to manage spatial stimuli) and mental rotation (the ability to rotate spatial stimuli). Method. Eighty-seven participants with DS, aged between 7 and 53 years (forty-seven males and forty females), completed spatial visualization and mental rotation tasks. Changes in these two abilities were analyzed in relation to chronological age and developmental level, the latter derived from Raven’s Colored Progressive Matrices. Results. Chronological age was linearly associated with spatial visualization performance, whereas mental rotation performance increased until 14 years of age and then decreased. Developmental level was linearly associated with increased performance in spatial visualization, the trend in mental rotation was segmented with an increase after 5 years of age. Furthermore, developmental trajectories in mental rotation depended on the rotation degree. Conclusion. Chronological age explains a modest quote of variance. Developmental level better describes changes in spatial visualization and mental rotation of individuals with DS. Full article
(This article belongs to the Special Issue Individuals with Down Syndrome)
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15 pages, 6556 KiB  
Article
Everyday Memory in People with Down Syndrome
by Yingying Yang, Zachary M. Himmelberger, Trent Robinson, Megan Davis, Frances Conners and Edward Merrill
Brain Sci. 2021, 11(5), 551; https://doi.org/10.3390/brainsci11050551 - 27 Apr 2021
Cited by 2 | Viewed by 2091
Abstract
Although memory functions in people with Down Syndrome (DS) have been studied extensively, how well people with DS remember things about everyday life is not well understood. In the current study, 31 adolescents/young adults with DS and 26 with intellectual disabilities (ID) of [...] Read more.
Although memory functions in people with Down Syndrome (DS) have been studied extensively, how well people with DS remember things about everyday life is not well understood. In the current study, 31 adolescents/young adults with DS and 26 with intellectual disabilities (ID) of mixed etiology (not DS) participated. They completed an everyday memory questionnaire about personal facts and recent events (e.g., school name, breakfast). They also completed a standard laboratory task of verbal long-term memory (LTM) where they recalled a list of unrelated words over trials. Results did not indicate impaired everyday memory, but impaired verbal LTM, in people with DS relative to people with mixed ID. Furthermore, the laboratory verbal LTM task predicted everyday memory for both groups after taking into account mental age equivalent. Our research showed both an independence and a connection between everyday memory and the standard laboratory memory task and has important research and clinical implications. Full article
(This article belongs to the Special Issue Individuals with Down Syndrome)
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21 pages, 374 KiB  
Article
Differences and Similarities in Predictors of Expressive Vocabulary Development between Children with Down Syndrome and Young Typically Developing Children
by Kari-Anne B. Næss, Johanne Ostad and Egil Nygaard
Brain Sci. 2021, 11(3), 312; https://doi.org/10.3390/brainsci11030312 - 02 Mar 2021
Cited by 8 | Viewed by 4091
Abstract
The purpose of this study was to examine potential differences in the predictors of expressive vocabulary development between children with Down syndrome and typically developing children to support preparation for intervention development. An age cohort of 43 children with Down syndrome and 57 [...] Read more.
The purpose of this study was to examine potential differences in the predictors of expressive vocabulary development between children with Down syndrome and typically developing children to support preparation for intervention development. An age cohort of 43 children with Down syndrome and 57 typically developing children with similar nonverbal mental age levels were assessed at three time points. Linear mixed models were used to investigate the predictors of expressive vocabulary over time. Both groups achieved progress in expressive vocabulary. The typically developing children had steeper growth than the children with Down syndrome (1.38 SD vs. 0.8 SD, p < 0.001). In both groups, receptive vocabulary, auditory memory, and the home literacy environment were significant predictors of development. In the children with Down syndrome, the phonological awareness and oral motor skills were also significant. Group comparisons showed that receptive vocabulary, auditory memory and oral motor skills were stronger predictors in the children with Down syndrome than in the typically developing children. These results indicate that children with Down syndrome are more vulnerable when it comes to risk factors that are known to influence expressive vocabulary than typically developing children. Children with Down syndrome therefore require early broad-based expressive vocabulary interventions. Full article
(This article belongs to the Special Issue Individuals with Down Syndrome)
13 pages, 283 KiB  
Article
Early Regulatory Skills and Social Communication Development in Infants with Down Syndrome
by Emily K. Schworer, Deborah J. Fidler and Lisa A. Daunhauer
Brain Sci. 2021, 11(2), 208; https://doi.org/10.3390/brainsci11020208 - 09 Feb 2021
Cited by 7 | Viewed by 2632
Abstract
Children with Down syndrome (DS) demonstrate substantial variability in communication and language outcomes. One potential source of variability in this skill area may be early regulatory function. Characterizing the early link between regulatory function and early social communication may benefit infants with DS [...] Read more.
Children with Down syndrome (DS) demonstrate substantial variability in communication and language outcomes. One potential source of variability in this skill area may be early regulatory function. Characterizing the early link between regulatory function and early social communication may benefit infants with DS at risk of difficulties with social communication and language skill acquisition. Forty-three infants with DS were assessed at two time points, six months apart. At Time 1, the average chronological age was 9.0 months (SD = 3.9) and caregivers completed the Infant Behavior Questionnaire-Revised (IBQ-R) to assess regulatory function. Six months later, caregivers rated infant communication at the second visit using the Communication and Symbolic Behavior Scales Infant Toddler Checklist (CSBS-ITC). Infant developmental level was assessed at both visits using the Bayley Scales of Infant and Toddler Development, Third Edition and caregivers reported on developmental history and biomedical comorbidities. Infant regulatory function at Time 1 predicted social communication outcomes at Time 2, six months later. Findings from this study suggest that elevated risk for pronounced communication challenges may be detectable as early as infancy in DS. Full article
(This article belongs to the Special Issue Individuals with Down Syndrome)
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