| Description |
1 online resource (xiv, 507 pages) : illustrations |
| Series |
Issues in clinical and cognitive neuropsychology |
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Issues in clinical and cognitive neuropsychology.
|
| Contents |
Turner syndrome in childhood / Marsha L. Davenport, Stephen R. Hooper and Martha Zeger -- Klinefelter syndrome / Judith L. Ross, Gerry A. Stefanatos and David Roeltgen -- Fragile X syndrome : the journey from genes to behavior / Kimberly M. Cornish, Andrew Levitas and Vicki Sudhalter -- Duchenne muscular dystrophy / Veronica J. Hinton and Edward M. Goldstein -- Neurofibromatosis / John M. Slopis and Bartlett D. Moore III -- Cognitive and behavioral characteristics of children with chromosome 22q11.2 deletion syndrome / Tony J. Simon, Merav Burg-Malki and Doron Gothelf -- Williams Syndrome / Carolyn B. Mervis and Colleen A. Morris -- Congenital hypothyroidism : genetic and biochemical influences on brain development and neuropsychological functioning / Joanne F. Rovet and Rosalind Brown -- Inborn errors of metabolism / Kevin M. Antshel and Georgianne Arnold -- Neurodevelopmental effects of childhood exposure to heavy metals : lessons from pediatric lead poisoning / Theodore I. Lidsky, Agnes T. Heaney, Jay S. Schneider and John F. Rosen -- Beyond the diagnosis : the process of genetic counseling / Allyn McConkie-Rosell and Julianne O'Daniel -- From diagnosis to adaptation : optimizing family and child functioning when a genetic diagnosis is associated with mental retardation / Laraine Masters Glidden and Sarah A. Schoolcraft -- When a genetic disorder is associated with learning disabilities / Michele M.M. Mazzocco -- Early intervention and early childhood special education for young children with neurogenetic disorders / Deborah D. Hatton -- The individualized education program : navigating the IEP development process / Vicki Sudhalter |
| Summary |
A reference to guide clinicians, researchers, teachers, and parents in identifying a range of genetic disorders despite widely variable cognitive, behavioral, and physical effects |
| Analysis |
NEUROSCIENCE/General |
| Bibliography |
Includes bibliographical references and index |
| Notes |
English |
|
Print version record |
| Subject |
Developmental disabilities -- Genetic aspects
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Chromosome abnormalities.
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Neurogenetics.
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Pediatric neuropsychology.
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Medical genetics.
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Nervous system -- Diseases.
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Abnormalities, Human.
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National health services.
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Diseases.
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Biology.
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Life sciences.
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Medical care.
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Physical sciences.
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Genetic disorders.
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Genetic counseling.
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Methodology.
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Diagnosis.
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Children.
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Congenital, Hereditary, and Neonatal Diseases and Abnormalities
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Analytical, Diagnostic and Therapeutic Techniques and Equipment
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Investigative Techniques
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Age Groups
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Chromosome Disorders
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Genetics, Medical
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Neurodegenerative Diseases
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Genetic Services
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Persons
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Nervous System Diseases
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Congenital Abnormalities
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Health Services
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Disease
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Genetics
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Health Care Facilities, Manpower, and Services
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Named Groups
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Biology
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Biological Science Disciplines
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Delivery of Health Care
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Natural Science Disciplines
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Disciplines and Occupations
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Heredodegenerative Disorders, Nervous System
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Genetic Diseases, Inborn
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Genetic Counseling
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Sex Chromosome Disorders
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Methods
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Diagnosis
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Genetic Diseases, Inborn -- diagnosis
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Child
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Genetic Counseling -- methods
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Heredodegenerative Disorders, Nervous System -- diagnosis
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Sex Chromosome Disorders -- diagnosis
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Chromosome Aberrations
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Patient Care
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biology.
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biological sciences.
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physical sciences.
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methodology.
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diagnosis.
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children (people by age group)
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Physical sciences
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Nervous system -- Diseases
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National health services
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Methodology
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Medical genetics
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Medical care
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Life sciences
|
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Genetic disorders
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Genetic counseling
|
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Diseases
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Diagnosis
|
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Children
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Biology
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Abnormalities, Human
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Chromosome abnormalities
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Developmental disabilities -- Genetic aspects
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Neurogenetics
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Pediatric neuropsychology
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| Genre/Form |
Aufsatzsammlung.
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| Form |
Electronic book
|
| Author |
Mazzocco, Michèle M. M.
|
|
Ross, Judith L.
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| ISBN |
9780262279321 |
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0262279320 |
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9781429477154 |
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1429477156 |
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1282098853 |
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9781282098855 |
|
