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        691-700 of 1299 results for 'Autism'

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        Research

        Intellectual disability: Population-based estimates of the proportion attributable to maternal alcohol use disorder during pregnancy

        The aim of this study was to examine the association between maternal alcohol use disorder and intellectual disability in children. ...

        News & Events

        New study links testosterone levels in the womb and language problems

        New study links testosterone levels in the womb and language problems ...

        Research

        Validating the Communication and Symbolic Behavior Scales–Developmental Profile Infant–Toddler Checklist (CSBS–DP ITC) Beyond Infancy in the CDKL5 Deficiency Disorder

        CDKL5 deficiency disorder (CDD) results in early-onset epilepsy and lifelong cognitive and motor impairments. With no validated measure for communication in CDD, this study evaluated the psychometric properties of the Communication and Symbolic Behavior Scales-Developmental Profile Infant Toddler Checklist. ...

        Research

        Use of health services in the last year of life and cause of death in people with intellectual disability: a retrospective matched cohort study

        People with intellectual disability were more likely to experience potentially preventable conditions at the end of their lives ...

        Research

        Intellectual disability in children conceived using assisted reproductive technology

        The risk of intellectual disability was increased in children born after assisted reproductive technology in Western Australia from 1994 to 2002 ...

        Research

        Young adults with intellectual disability transitioning from school to post-school: A literature review framed within the ICF

        The purpose of this review was to describe literature relating to transition for young people with an intellectual disability and identify knowledge base gaps. ...

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        Sarah Pillar

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        Research

        Exploring quality of life in individuals with a severe developmental and epileptic encephalopathy, CDKL5 Deficiency Disorder

        CDKL5 Deficiency Disorder (CDD) is a rare genetic disorder caused by a mutation in the cyclin-dependent kinase-like 5 (CDKL5) gene. It is now considered to be a developmental and epileptic encephalopathy because of the early onset of seizures in association with severe global delay. Other features include cortical visual impairment, sleep and gastro-intestinal problems. Progress in clinical understanding, especially regarding the spectrum of functional ability, seizure patterns, and other comorbidities was initially slow but accelerated in 2012 with the establishment of the International CDKL5 Database (ICDD). Our aim was to use this data source to investigate quality of life (QOL) and associated factors in this disorder. ...

        Research

        A framework for understanding quality of life domains in individuals with the CDKL5 deficiency disorder

        This study aimed to identify the quality of life domains important for individuals with CDKL5 deficiency disorder ...

        Research

        Caregiver Perspective of Benefits and Side Effects of Anti-Seizure Medications in CDKL5 Deficiency Disorder from an International Database

        CDKL5 deficiency disorder presents as a challenging condition with early-onset refractory seizures, severe developmental delays, and a range of other neurological symptoms. Our study aimed to explore the benefits and side effects of anti-seizure medications in managing seizures among individuals with CDKL5 deficiency disorder, drawing on data from the International CDKL5 Disorder Database.   ...

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