Neurogenetic developmental disorders : variation of manifestation in childhood / edited by Michèle M.M. Mazzocco and Judith L. Ross.

Contributor(s): Mazzocco, Michèle M. M | Ross, Judith L
Material type: TextTextSeries: Issues in clinical and cognitive neuropsychology: Copyright date: ©2007Description: 1 online resource (xiv, 507 pages) : illustrationsContent type: text Media type: computer Carrier type: online resourceISBN: 9780262279321; 0262279320; 9781429477154; 1429477156; 1282098853; 9781282098855Subject(s): Developmental disabilities -- Genetic aspects | Chromosome abnormalities | Neurogenetics | Pediatric neuropsychology | Congenital, Hereditary, and Neonatal Diseases and Abnormalities | Analytical, Diagnostic and Therapeutic Techniques and Equipment | Investigative Techniques | Age Groups | Chromosome Disorders | Genetics, Medical | Neurodegenerative Diseases | Genetic Services | Persons | Nervous System Diseases | Congenital Abnormalities | Health Services | Disease | Genetics | Health Care Facilities, Manpower, and Services | Named Groups | Biology | Biological Science Disciplines | Delivery of Health Care | Natural Science Disciplines | Disciplines and Occupations | Heredodegenerative Disorders, Nervous System | Genetic Diseases, Inborn | Genetic Counseling | Sex Chromosome Disorders | Methods | Diagnosis | Genetic Diseases, Inborn -- diagnosis | Child | Genetic Counseling -- methods | Heredodegenerative Disorders, Nervous System -- diagnosis | Sex Chromosome Disorders -- diagnosis | Chromosome abnormalities | Developmental disabilities -- Genetic aspects | Neurogenetics | Pediatric neuropsychology | NEUROSCIENCE/GeneralGenre/Form: Electronic books. | Electronic books. | Aufsatzsammlung. Additional physical formats: Print version:: Neurogenetic developmental disorders.DDC classification: 618.92/8588 LOC classification: RJ506.D47 | N486 2007Online resources: Click here to access online
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.
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Includes bibliographical references and index.

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.

Print version record.

A reference to guide clinicians, researchers, teachers, and parents in identifying a range of genetic disorders despite widely variable cognitive, behavioral, and physical effects.

English.

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