Handbook of Neurodevelopmental and Genetic Disorders in Children, 2/eSam Goldstein, Cecil R. Reynolds Recognized as the definitive reference in the field, this book addresses a broad range of biologically based disorders that affect children's learning and development. Leading authorities review the genetics of each disorder; its course and outcome; associated developmental, cognitive, and psychosocial challenges; and what clinicians and educators need to know about effective approaches to assessment and intervention. Coverage encompasses more frequently diagnosed learning and behavior problems with a genetic component as well as numerous lower-incidence neurodevelopmental disabilities. Illustrations include 12 color plates. |
Contents
Chapter 17 | 322 |
Chapter 18 | 338 |
Chapter 19 | 362 |
Chapter 20 | 382 |
Chapter 21 | 398 |
Chapter 22 | 425 |
Chapter 23 | 445 |
Chapter 24 | 460 |
Chapter 9 | 171 |
Chapter 10 | 188 |
Chapter 11 | 209 |
Chapter 12 | 228 |
Chapter 13 | 261 |
Chapter 14 | 276 |
Chapter 15 | 293 |
Chapter 16 | 311 |
Chapter 25 | 484 |
512 | |
Chapter 27 | 539 |
554 | |
570 | |
579 | |
Plates | 590 |
Other editions - View all
Handbook of Neurodevelopmental and Genetic Disorders in Children, 2/e Sam Goldstein,Cecil R. Reynolds No preview available - 2010 |
Handbook of Neurodevelopmental and Genetic Disorders in Children, 2/e Sam Goldstein,Cecil R. Reynolds No preview available - 2010 |
Common terms and phrases
abnormalities academic Academy of Child ADHD Adolescent Psychiatry adults American Journal anxiety disorders assessment associated autism behavior bipolar disorders brain chil Child and Adolescent Child Neurology childhood children and adolescents chromosome clinical cognitive colleagues comorbid deficits depression developmental diagnosis dren drome Dykens early effects epilepsy factors fragile X syndrome frontal functioning gene Hagerman hyperactivity identified impairment increased individuals intervention Journal of Child language learning disabilities levels lissencephaly lobe males MECP2 Medical Genetics memory ment mental retardation metabolic mitochondrial mitochondrial disease motor MPS disorders mtDNA mutations neuroimaging Neurology neuropsychological normal onset parents patients Pediatrics phenotype phenylalanine phenylketonuria Prader–Willi syndrome prevalence problems processing Psychology rates reported Rett syndrome risk Schatz schizencephaly scores seizures sickle cell disease skills social specific symptoms testing therapy tics tion tive Tourette syndrome treatment Turner syndrome white matter