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        553-564 of 965 results for 'autism'

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        A qualitative investigation of recovery after femoral fracture in Rett syndrome

        Jenny Helen Downs Leonard JA HM BApplSci (physio) MSc PhD MBChB MPH Program Head, Development and Disability Principal Research Fellow 08 6319 1763 +61 419 956 946 Jenny.Downs@telethonkids.org.au helen.leonard@telethonkids.org.au Head, Child ...

        Research

        Child protection involvement of children of mothers with intellectual disability

        Children born to parents with intellectual disability (ID) have been shown as disproportionally represented in child protection services however with limited population-based research. ...

        Research

        Predictors of seizure onset in Rett syndrome

        Information on presence and age at onset of seizures, perinatal and developmental history, and genetic status was abstracted on 275 cases in the Australian... ...

        Research

        An investigation of the determinants of quality of life in adolescents and young adults with Down syndrome

        Quality of life of young people with Down syndrome was most negatively associated with burden of medical conditions, but also with lack of friendships ...

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        Young people with intellectual disability transitioning to adulthood: Do behaviour trajectories differ in those with and without down syndrome

        Changes in emotional and behavioural problems for young people with intellectual disability with and without Down syndrome as they transition into adulthood ...

        Research

        Impact of Gastrostomy Placement on Nutritional Status, Physical Health, and Parental Well-Being of Females with Rett Syndrome

        Gastrostomy placement was associated with improvement in BMI in females with Rett syndrome, but its long-term impact on individuals and their families is unclear ...

        Research

        Adapting a measure of gross motor skills for individuals with CDKL5 deficiency disorder: A psychometric study

        Validated measures capable of demonstrating meaningful interventional change in the CDKL5 deficiency disorder (CDD) are lacking. The study objective was to modify the Rett Syndrome Gross Motor Scale (RSGMS) and evaluate its psychometric properties for individuals with CDD. ...

        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. ...

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        The incidence, prevalence and clinical features of MECP2 duplication syndrome in Australian children

        MECP2 duplication syndrome is a rare but important diagnosis in children because of the burden of respiratory illness and recurrence risk ...

        Research

        Use of the ketogenic diet to manage refractory epilepsy in CDKL5 disorder

        In view of its side effect profile, ketogenic diet (KD) administration should be supervised by a pediatric neurologist and specialist dietician. ...

        Research

        Patterns of depressive symptoms and social relating behaviors differ over time from other behavioral domains for young people with Down syndrome

        People with intellectual disabilities are at a higher risk for experiencing behavioral, emotional, and psychiatric problems in comparison with the general... ...

        Research

        Clinical guidelines for management of bone health in rett syndrome based on expert consensus and available evidence

        A clinically significant history of fracture in combination with low bone densitometry findings is necessary for a diagnosis of osteoporosis in Rett Syndrome ...

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