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Chugani, Diane C. – Mental Retardation and Developmental Disabilities Research Reviews, 2004
Serotonergic abnormalities have been reported in both autism and epilepsy. This association may provide insights into underlying mechanisms of these disorders because serotonin plays an important neurotrophic role during brain development--and there is evidence for abnormal cortical development in both autism and some forms of epilepsy. This…
Descriptors: Epilepsy, Autism, Brain, Metabolism
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Zigman, Warren B.; Lott, Ira T. – Mental Retardation and Developmental Disabilities Research Reviews, 2007
Down syndrome (DS) is characterized by increased mortality rates, both during early and later stages of life, and age-specific mortality risk remains higher in adults with DS compared with the overall population of people with mental retardation and with typically developing populations. Causes of increased mortality rates early in life are…
Descriptors: Heart Disorders, Alzheimers Disease, Mortality Rate, Down Syndrome
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Sen, Ellora; Levison, Steven W. – Mental Retardation and Developmental Disabilities Research Reviews, 2006
There is an increasing awareness that the astrocytes in the immature periventricular white matter are vulnerable to ischemia and respond to inflammation. Here we provide a synopsis of the articles that have evaluated the causes and consequences of developmental brain injuries to white matter astrocytes as well as the consequences of several…
Descriptors: Injuries, Literature Reviews, Brain, Disabilities
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Kumar, Shalini; Mattan, Natalia S.; de Vellis, Jean – Mental Retardation and Developmental Disabilities Research Reviews, 2006
Breakdown of oligodendrocyte-neuron interactions in white matter (WM), such as the loss of myelin, results in axonal dysfunction and hence a disruption of information processing between brain regions. The major feature of leukodystrophies is the lack of proper myelin formation during early development or the onset of myelin loss late in life.…
Descriptors: Diseases, Genetics, Brain, Developmental Stages
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DeBaun, Michael R.; Derdeyn, Colin P.; McKinstry, Robert C., III – Mental Retardation and Developmental Disabilities Research Reviews, 2006
The most devastating complication of sickle cell anemia is cerebral infarction, affecting [approximately]30% of all individuals with sickle cell anemia. Despite being one of the most common causes of stroke in infants and children, the mechanism of cerebral infarction in this population has not been extensively studied and is poorly understood.…
Descriptors: Diseases, At Risk Persons, Etiology, Epidemiology
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Darnell, Jennifer C.; Warren, Stephen T.; Darnell, Robert B. – Mental Retardation and Developmental Disabilities Research Reviews, 2004
Fragile X mental retardation is a disease caused by the loss of function of a single RNA-binding protein, FMRP. Identifying the RNA targets recognized by FMRP is likely to reveal much about its functions in controlling some aspects of memory and behavior. Recent evidence suggests that one of the predominant RNA motifs recognized by the FMRP…
Descriptors: Mental Retardation, Genetics, Genetic Disorders, Cognitive Ability
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Malow, Beth A. – Mental Retardation and Developmental Disabilities Research Reviews, 2004
The purpose of this review article is to describe the clinical data linking autism with sleep and epilepsy and to discuss the impact of treating sleep disorders in children with autism either with or without coexisting epileptic seizures. Studies are presented to support the view that sleep is abnormal in individuals with autistic spectrum…
Descriptors: Epilepsy, Autism, Seizures, Sleep
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Levy, Susan E.; Hyman, Susan L. – Mental Retardation and Developmental Disabilities Research Reviews, 2005
In no area of developmental pediatric practice is there more controversy regarding the choice of treatment than related to children with autistic spectrum disorders (ASD). Complementary and alternative medical therapies (CAM) are often elected because they are perceived as treating the cause of symptoms rather than the symptoms themselves. CAM…
Descriptors: Autism, Therapy, Pervasive Developmental Disorders, Children
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Brosco, Jeffrey P.; Seider, Michael I.; Dunn, Angela C. – Mental Retardation and Developmental Disabilities Research Reviews, 2006
Universal newborn screening programs for metabolic disorders are typically described as a triumph of medicine and public policy in the US over the last 50 years. Advances in science and technology, including the Human Genome Project, offer the opportunity to expand universal newborn screening programs to include many additional metabolic and…
Descriptors: Medical Services, Test Results, Screening Tests, Diseases
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James, Philip M.; Levy, Harvey L. – Mental Retardation and Developmental Disabilities Research Reviews, 2006
The aim of newborn screening is to identify presymptomatic healthy infants that will develop significant metabolic or endocrine derangements if left undiagnosed and untreated. The goal of ultimately reducing or eliminating irreversible sequelae is reached by maximizing test sensitivity of the primary newborn screening that measures specific…
Descriptors: Therapy, Screening Tests, Neonates, Infant Care
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Beckel-Mitchener, Andrea; Greenough, William T. – Mental Retardation and Developmental Disabilities Research Reviews, 2004
Fragile X syndrome (FXS) is characterized by a pattern of morphological, functional, and molecular characteristics with, in at least some cases, apparent relationships among phenotypic features at different levels. Gross morphology differences in the sizes of some human brain regions are accompanied by fine structural alterations in the shapes and…
Descriptors: Brain, Cognitive Processes, Molecular Structure, Genetic Disorders
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DiPietro, Janet A. – Mental Retardation and Developmental Disabilities Research Reviews, 2005
The complexities of neurobehavioral assessment of the fetus, which can be neither directly viewed nor manipulated, cannot be understated. Impetus to develop methods for measuring fetal neurobehavioral development has been provided by the recognition that individual differences in neurobehavioral functioning do not originate with birth and…
Descriptors: Metabolism, Stimulation, Predictive Validity, Pregnancy
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Sundaram, Senthil K.; Chugani, Harry T.; Chugani, Diane C. – Mental Retardation and Developmental Disabilities Research Reviews, 2005
Positron emission tomography (PET) is a technique that enables imaging of the distribution of radiolabeled tracers designed to track biochemical and molecular processes in the body after intravenous injection or inhalation. New strategies for the use of radiolabeled tracers hold potential for imaging gene expression in the brain during development…
Descriptors: Genetic Disorders, Mental Retardation, Developmental Disabilities, Genetics