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Maria Lepore-Stevens; Arielle Sosland – Journal of Visual Impairment & Blindness, 2025
Introduction: Albinism is a genetic condition caused by a lack of pigment in the eyes, with some forms of albinism also affecting pigmentation in the hair and skin. Individuals with albinism experience some degree of visual impairment as well as hypopigmentation. Both visual impairment and physical appearance may contribute to students with…
Descriptors: Genetic Disorders, Students with Disabilities, Visual Impairments, Inclusion
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Harvey, Hannah; Ashworth, Maria; Palikara, Olympia; Van Herwegen, Jo – Journal of Autism and Developmental Disorders, 2020
Vision problems can lead to negative developmental outcomes. Children with Williams syndrome and Down syndrome are at higher risk of vision problems, and these are less likely to be detected due to diagnostic overshadowing and difficulty accessing eye-care. Education, Health and Care (EHC) plans are statutory documents, introduced by the Children…
Descriptors: Visual Impairments, Genetic Disorders, Down Syndrome, Children
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Van Herwegen, Jo; Ranzato, Erica; Karmiloff-Smith, Annette; Simms, Victoria – Journal of Applied Research in Intellectual Disabilities, 2020
Background: Studies in Down syndrome (DS) and Williams syndrome (WS) have suggested that mathematical abilities are impaired. However, it is unclear which domain-general or domain-specific abilities impact on mathematical development in these developmental disorders. Method: The current study examined the foundations of mathematical development…
Descriptors: Numeracy, Number Concepts, Mathematics Skills, Genetic Disorders
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Thom, Robyn P.; Keary, Christopher J.; Waxler, Jessica L.; Pober, Barbara R.; McDougle, Christopher J. – Journal of Autism and Developmental Disorders, 2020
Co-morbid anxiety disorders, including generalized anxiety disorder (GAD), are highly prevalent among individuals with Williams syndrome (WS). However, reports of the pharmacologic treatment of only a limited number of previous anxiety disorders in WS have appeared in the literature. Here, we review the case histories of three adolescents/young…
Descriptors: Anxiety Disorders, Genetic Disorders, Drug Therapy, Adolescents
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Simms, V.; Karmiloff-Smith, A.; Ranzato, E.; Van Herwegen, J. – Journal of Autism and Developmental Disorders, 2020
Previous studies suggest that tasks dependent on the mental number line may be difficult for Williams Syndrome (WS) and Down Syndrome (DS) groups. However, few have directly assessed number line estimation in these groups. The current study assessed 28 WS, 25 DS and 25 typically developing (TD) participants in non-verbal intelligence, number…
Descriptors: Genetic Disorders, Down Syndrome, Computation, Numbers
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Magdalena Glod; Deborah M. Riby; Jacqui Rodgers – Review Journal of Autism and Developmental Disorders, 2020
To date, little is known about sensory processing in Williams syndrome (WS) and the similarities of the sensory profile in individuals with WS compared to people with other neurodevelopmental disorders. The current review aims to consolidate available evidence on sensory processing in WS. Eighteen primary studies investigating sensory processing…
Descriptors: Genetic Disorders, Developmental Disabilities, Perceptual Impairments, Age Differences
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Ümran Betül Cebesoy; Banuçiçek Seyhan Özdemir – Turkish Journal of Education, 2024
Socioscientific (SSI)-based instruction has gained popularity in science education research as the number of controversial topics has increased daily. This study has two objectives: first, it aims to explore the quality of arguments made by pre-service science teachers (PSTs) through various SSI contexts. Second, it explores whether the context…
Descriptors: Preservice Teacher Education, Preservice Teachers, Science Teachers, Science and Society
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Kirchner, Rebecca M.; Walton, Katherine M. – American Journal on Intellectual and Developmental Disabilities, 2021
Research suggests that people with a Williams syndrome (WS) or Down syndrome (DS) diagnosis display an increased prevalence of autism spectrum disorder (ASD) when compared to the general population. This study aimed to examine characteristics of ASD in a group of children with DS or WS. Results suggest that children with DS and WS exhibit higher…
Descriptors: Symptoms (Individual Disorders), Autism, Pervasive Developmental Disorders, Down Syndrome
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Gillooly, Amanda E.; Riby, Deborah M.; Durkin, Kevin; Rhodes, Sinéad M. – Journal of Autism and Developmental Disorders, 2021
Although children with Williams syndrome (WS) are reported to show a strong motivation towards social interaction, evidence suggests many experience difficulties with peer relations. Less is known regarding the characteristics of such difficulties. Parents and teachers of 21 children with WS (7- to 16 years) completed questionnaires measuring…
Descriptors: Peer Relationship, Children, Adolescents, Parent Attitudes
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Buijs, Petra C. M.; Bassett, Anne S.; Gold, David A.; Boot, Erik – Journal of Intellectual Disabilities, 2021
Background: The prevalence of anxiety disorders is high in 22q11.2 deletion syndrome (22q11.2DS), an under-recognized multisystem condition. Prominent features include an array of somatic, cognitive, and neuropsychiatric disorders. This case study reports for the first time on the application of individual cognitive behavioral therapy in…
Descriptors: Anxiety Disorders, Genetic Disorders, Symptoms (Individual Disorders), Cognitive Restructuring
Donna J. Romack – ProQuest LLC, 2023
Sickle cell disease (SCD) is a lifelong chronic medical condition diagnosed through screening at birth. Complications of SCD can significantly burden affected children as they learn to manage their health needs. This study sought to investigate the perceived obstacles that may hinder children with SCD from receiving the necessary support and…
Descriptors: Genetic Disorders, Chronic Illness, Barriers, Children
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Rikken-Evers, M. T.; Smith, K. D.; Sterkenburg, P. S. – Journal of Intellectual Disabilities, 2022
Aims: To assess the effectiveness of iPad use on the attention span of a child with Smith Magenis Syndrome (n = 1), compared to attention span while working on the same tasks manually. Methods: An AB design with a baseline and an intervention phase was used. Three manual tasks were chosen for the baseline, which matched the participant's…
Descriptors: Genetic Disorders, Handheld Devices, Telecommunications, Program Effectiveness
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Block, Elisa; Farran, Emily K.; Van Herwegen, Jo – American Journal on Intellectual and Developmental Disabilities, 2022
The block design task (BDT) is a visuospatial measure that individuals with Williams syndrome (WS) perform poorly on. However, it is unclear what underlies their impaired performance. This study investigated whether poorer performance is a result of visuospatial difficulties, executive function (EF) difficulties, atypical looking strategies, or a…
Descriptors: Task Analysis, Visual Perception, Spatial Ability, Executive Function
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Agarwal, Rumi; Maddux, Marlaina; Marolda, Heather; Quintana, Jordan; Wagner, Eric; Burke, Shanna – International Journal of Disability, Development and Education, 2022
Programmes which offer integrated services were analysed to identify model international and domestic programmes serving adults with neurodevelopmental disorders. Programmes were assessed according to 11 need domains identified in a previous study: supervision, transportation, housing, communication, finances/employment opportunities, activities…
Descriptors: Adults, Program Evaluation, Neurological Impairments, Developmental Disabilities
Cynde Katherine Josol – ProQuest LLC, 2022
Empathy is generally described as a multidimensional construct, consisting of cognitive and affective components. Researchers demonstrate that a better ability to understand and express empathy toward others is associated with positive social outcomes such as strong communication skills and meaningful social relationships. For individuals with…
Descriptors: Empathy, Affective Behavior, Intellectual Disability, Developmental Disabilities
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