Williams-Beuren syndrome : research, evaluation, and treatment
著者
書誌事項
Williams-Beuren syndrome : research, evaluation, and treatment
Johns Hopkins University Press, 2006
大学図書館所蔵 全1件
  青森
  岩手
  宮城
  秋田
  山形
  福島
  茨城
  栃木
  群馬
  埼玉
  千葉
  東京
  神奈川
  新潟
  富山
  石川
  福井
  山梨
  長野
  岐阜
  静岡
  愛知
  三重
  滋賀
  京都
  大阪
  兵庫
  奈良
  和歌山
  鳥取
  島根
  岡山
  広島
  山口
  徳島
  香川
  愛媛
  高知
  福岡
  佐賀
  長崎
  熊本
  大分
  宮崎
  鹿児島
  沖縄
  韓国
  中国
  タイ
  イギリス
  ドイツ
  スイス
  フランス
  ベルギー
  オランダ
  スウェーデン
  ノルウェー
  アメリカ
注記
Includes bibliographical references and index
内容説明・目次
内容説明
Williams-Beuren syndrome (WBS) is a genetic condition characterized by low IQ, cardiovascular malformations, dysmorphic facial features, and a striking pattern of behaviors, weaknesses, and strengths, such as musical and verbal abilities, extraordinary friendliness, empathy, and social grace. Because the typical psychological and cognitive profile is unique, examination of this syndrome sheds light on how the human brain is organized and how different aspects of cognition and behavior arise. Williams-Beuren Syndrome offers concise, comprehensive coverage of WBS research and its clinical implications, including its genetics and molecular biology, neurobiological and behavioral traits, and medical problems and their management. Each chapter emphasizes how research can be applied to clinical practice.
The expertise of the volume editors ranges from pioneering research to personal experience: Colleen Morris played a key role in the breakthrough discovery of the missing elastin gene in patients with WBS; Howard Lenhoff is a biologist, an expert on WBS and musical pitch, and the parent of a WBS musical savant; Paul Wang is a pediatrician and cognitive researcher who works in the WBS community. Researchers and clinicians in genetics, pediatrics, and psychiatry/psychology will find in this volume a wealth of current information on WBS, as well as valuable insights into future research possibilities.
目次
Foreword by John C. Carey
Preface
Contributors
I. Biomedical and Genetic Research
1. The Dysmorphology, Genetics, and Natural History of Williams-Beuren Syndrome
2. The Molecular Basis of a Multisystem Disorder
3. Genotype-Phenotype Correlations in Williams-Beuren Syndrome
4. The Medical Management of Children with Williams-Beuren Syndrome
5. Cardiovascular Disease in Williams-Beuren Syndrome
6. Evidence-Based Medical Management of Adults with Williams-Beuren Syndrome
II. Behavioral Neuroscience Research
7. The Behavioral Neuroscience of Williams-Beuren Syndrome: An overview
8. Language Abilities in Williams-Beuren Syndrome
9. Specialization, Breakdown, and Sparing in Spatial Cognition: Lessons from Williams-Beuren Syndrome
10. Social Cognition in Williams-Beuren Syndrome
11. Theoretical Implications of Studying Cognitive Development in Genetic Disorders: The Case of Williams-Beuren Syndrome
12. Psychopathology in Persons with Williams-Beuren Syndrome
13. Sleep Pattens in Williams-Beuren Syndrome
14. The Neurobiology of Williams-Beuren Syndrome
15. Absolute Pitch and Neuroplasticity in Williams-Beuren Syndrome
16. Rhythm, Timbre, and Hyperacusis in Williams-Beuren Syndrome
Index
「Nielsen BookData」 より