Hospitalisation rates for epilepsy, asthma and insulin-dependent diabetes in 796 190 school-aged children and young people with and without intellectual disabilities: a record-linkage cohort study by Angela Henderson, Sally-Ann Cooper, Craig Melville, Michael Fleming, Gillian S Smith, Jill Pell, Deborah Cairns

“…Scotland’s Pupil Census, 2008–2013, was used to identify pupils with and without intellectual disabilities and was linked with the Prescribing Information Service to identify pupils with epilepsy, asthma and insulin-dependent diabetes, and the Scottish Morbidity Records-01 to identify hospital admissions.Setting The general child population of Scotland.Participants School pupils aged 4–19 years; 18 278 with intellectual disabilities and 777 912 without intellectual disabilities.Outcomes Overall, emergency and non-emergency hospitalisations for epilepsy, asthma and/or diabetes; and length of stay.Results Epilepsy and asthma were more prevalent in pupils with intellectual disabilities (8.8% and 8.9%, respectively, compared with 0.8% and 6.9% among pupils without intellectual disabilities, p<0.001), whereas insulin-dependent diabetes was not (0.5% prevalence). …”
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Comparison of Family Functioning, Maternal Mental Health and Maternal Coping Strategies, Between The Cases Who Are Diagnosed with Attention Deficit and Hyperactivity Disorder and The Cases Who Are Diagnosed with Intellectual Disability by Gonca Ozyurt, Yusuf Ozturk

“…Aim: Comparision of family functioning, maternal mental health and maternal coping strategies, between the cases who are diagnosed with attention deficit and hyperactivity disorder (ADHD) and the cases who are diagnosed with intellectual disability (ID) and controls, was aimed in this study. …”
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MORPHOSYNTACTIC ABILITIES IN CHILD WITH INTELETUAL DISABILITIES: CASE STUDY by Kumaralalitya Wisnu Pambayun, Agus Subiyanto

Subjects: “…Intellectual Disabilities…”
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Truncated SPAG9 as a novel candidate gene for a new syndrome: Coarse facial features, albinism, cataract and developmental delay (CACD syndrome) by Majid Alfadhel, Bashayr S. Alhubayshi, Muhammad Umair, Ahmed Alfaidi, Deemah Alwadaani, Essra Aloyouni, Safdar Abbas, Abdulkareem Al Abdulrahman, Mohammed Aldrees, Abeer Al Tuwaijri, Ruaa S. Alharithy, Abdulaziz Alajlan, Abdulrahman Alswaid, Saad Almohrij, Sultan Al-Khenaizan

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Forms and correlates of child maltreatment among autistic children involved in child protection services by Jacinthe Dion, Jacinthe Dion, Geneviève Paquette, Geneviève Paquette, Mireille De La Sablonnière-Griffin, Mireille De La Sablonnière-Griffin, Malena Argumedes, Alexa Martin-Storey, Alexa Martin-Storey, Marie-Louise Bolduc, Sonia Hélie, Ève-Line Bussières

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A subpopulation of cortical neurons altered by mutations in the autism risk gene DDX3X by Michael A. Flores, Marta Garcia-Forn, Alexa von Mueffling, Praise Ola, Yeaji Park, Andrea Boitnott, Silvia De Rubeis

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Handgrip strength measurement protocols in individuals with Down syndrome: a systematic review and meta-regression<subtitle>Handgrip strength measurement protocols and Down syndrom... by Geiziane L. R. Melo, Rafaela C. Espírito Santo, Viney P. Dubey, Cesar Agostinis-Sobrinho

Subjects: “…Intellectual disability…”
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Social robots in adult psychiatry: a summary of utilisation and impact by Maja Kling, Alfred Haeussl, Nina Dalkner, Frederike T. Fellendorf, Melanie Lenger, Alexander Finner, Julia Ilic, Irina S. Smolak, Lena Stojec, Ina Zwigl, Eva Z. Reininghaus

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Multidisciplinary, multicenter consensus for the care of patients affected with Sturge–Weber syndrome by May El Hachem, Andrea Diociaiuti, Angela Galeotti, Francesca Grussu, Elena Gusson, Alessandro Ferretti, Carlo Efisio Marras, Davide Vecchio, Simona Cappelletti, Mariasavina Severino, Carlo Gandolfo, Simone Reali, Rosa Longo, Carmen D’Amore, Lodovica Gariazzo, Federica Marraffa, Marta Luisa Ciofi Degli Atti, Maria Margherita Mancardi, and the Sturge-Weber Syndrome Multidisciplinary Group

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Case report: Discovery of novel CTNNB1 mutations and comparison of clinical characteristics in two patients with NEDSDV by Eojin Lee, Ja Young Choi, Shin-Seung Yang

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Case Report: The first Korean familial case of BCAP31-related deafness, dystonia, and cerebral hypomyelination by Yoong-A Suh, Jisun Hwang, Go Hun Seo, Rin Khang, Jang Hoon Lee, Moon Sung Park, Young Bae Sohn

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Clinical Features and Genetic Characteristics of XLID Patients With KDM5C Gene Mutations: Insights on Phenotype–Genotype Correlations From 175 Previous Cases and Identification of... by Mohammad‐Reza Ghasemi, Zahra Esmaeilizadeh, Sahand Tehrani Fateh, Hossein Sadeghi, Saman Bagheri, Farzad Hashemi‐Gorji, Morteza Sheikhi Nooshabadi, Rasoul Madannezhad, Toktam Sadat Tavabe Ghavami, Reza Mirfakhraie, Mohammad Miryounesi

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A transgenic cell line with inducible transcription for studying (CGG)n repeat expansion mechanisms by I. V. Grishchenko, A. A. Tulupov, Y. M. Rymareva, E. D. Petrovskiy, A. A. Savelov, A. M. Korostyshevskaya, Y. V. Maksimova, A. R. Shorina, E. M. Shitik, D. V. Yudkin

Subjects: “…hereditary intellectual disability…”
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Narrative microstructure and macrostructure in adolescents with Down syndrome and Williams syndrome by Aitana Viejo, Maite Fernández-Urquiza, Eliseo Diez-Itza

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Genome rearrangements in neurodevelopmental disorders of the central nervous system: origins, genomic mechanisms, functional and clinical consequences. Review article by V. Kučinskas, E. Preikšaitienė, L. Ambrozaitytė, L. Cimbalistienė, A. Utkus

“… Intellectual disability affects about 1-2% of the general population worldwide, and this is the leading socio-economic problem of the healthcare system. …”
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Dalle politiche assistenziali alle social farms: note sul dare, ricevere e ricambiare nel sistema di welfare sulla disabilità by Stefano Onnis

“… In this article I correlate the concept of gift ‒ referring to Marcel Mauss and his theory of giving-receiving-reciprocating ‒ with three specific areas in the field of intellectual disability: voluntary associations, cooperatives of social services and social cooperatives that promote employment opportunities for people with intellectual disability. …”
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Discovery of a Novel DYRK1A Mutation (c.524del) in Intellectual Development Disorder Autosomal Dominant 7 (MRD7): A Comprehensive Case Analysis by Fiona Whitaker, Alvaro Serrano

“…We report a case of DYRK1A-related intellectual disability syndrome caused by a novel mutation.…”
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A Boy With KIF11-Associated Disorder Along With ADHD and ASD: Collaboration Between Paediatrics and Child Psychiatry by Annelien Marcelis, Evelyne Van Reet

“…Kinesin family member 11 (KIF11)-associated disorder, a rare condition caused by autosomal dominant mutations in the KIF11 gene, presents with microcephaly, chorioretinal dysplasia, lymphoedema, and varying degrees of intellectual disability. While intellectual disability is often described in the literature on KIF11 mutations, autism spectrum disorder (ASD) and attention-deficit/hyperactivity disorder (ADHD) are only mentioned by a few authors but not thoroughly investigated. …”
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Inclusively Designing for People in Human-Robot Collaboration. by Laurianne Sitbon, Saminda Balasuriya, Alicia Mitchell

“… This article offers the perspectives of adults with intellectual disability on how future trends, particularly in social robotics, but also in collaborative robotics, can be co-designed inclusively. …”
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A Case of DeSanto-Shinawi Syndrome in Bahrain with a Novel Mutation by Zahra Alsahlawi, Mohamed Jailani, Husain Alaradi, Abdulaziz AlAbbad

“…This patient also showed signs of intellectual disability and behavioral abnormalities such as night terrors. …”
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