Neural Tube Defects:From origin to treatment

Neural Tube Defects:From origin to treatment

神经管缺陷：从发病到治愈
医学遗传学

原价：

￥ 2406.25

售价：

优惠

平台大促低至8折优惠

发货周期：预计5-7周发货

作者

Wyszynski, Diego F.

出版社

Oxford University Press

出版时间

2005年11月03日

装帧

精装

ＩＳＢＮ

9780195166033

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页码

417

开本

278x214mm

语种

英文

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暂无评分

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图书简介

Neural tube defects affect about 4000 pregnancies a year and are thus among the most common of severe birth defects. Prenatal diagnosis can now detect about 70% of neural tube defects, but the tests produce many false positives, so the question is under what circumstances should they be recommended to pregnant women. This comprehensive volume - the collective knowledge of more than fifty-five experts in the field - provides lucid and authoritative discussions on this topic as well as on a wide variety of theoretical, experimental and clinical issues. It addresses embryology, epidemiology, genetics, clinical features of NTDs, surgical techniques, treatment and patient educations, and public health. Written with a wide readership in mind, the book will be of interest to geneticists, pediatricians, neurologists, internists, graduate students, researchers interested in the field of birth defects, as well as to individuals with NTDs and their family members.

Foreword; Section I: Basic principles; Part 1: Clinical and molecular embryology of the central nervous system; 1: Neural crest formation; 2: The embryonic basis of neural tube defects; 3: The zebrafish as a model for analyzing neural tube defects; 4: Genetic regulation of early nervous system development; Part 2: Clinical features of neural tube defects; 5: Physical examination of the spine; 6: Classification of neural tube defects; 7: Syndromes with neural tube defects; 8: The tethered cord syndrome; 9: Prenatal screening and diagnosis of neural tube defects; Part 3: Epidemiology of neural tube defects; 10: Methodological issues in the study of neural tube defects; 11: Birth defects surveillance systems and neural tube defects; 12: An international perspective on anencephaly and spina bifida: Prevalences by the turn of the century; 13: Maternal exposure to selected environmental factors and risk for neural tube defects in the offspring; Part 4: Genetics of neural tube defects; 14: Nonsyndromic neural tube defects: genetic basis and genetic investigations; 15: Genetic risk factors for neural tube defects: variants in folate metabolism; 16: Genetics of syndromic neural tube defects; 17: Mouse mutants as models of neural tube defects; Section II: Treatment and education; 18: Fetal surgery for myelomeningocele; 19: Postnatal surgery for myelomeningocele; 20: Neurosurgical management of adults with spina bifida; 21: Orthopedic surgery; 22: Urological care and management of patients with neural tube defects; 23: Cognition, education and learning disorders; 24: Transition to adulthood; 25: Transition/toilet training, and sexuality; 26: Psychological adjustment and family relationships in children and adolescents with spina bifida; 27: When and how to communicate to people with spina bifida and their families; 28: Genetic counselling and interpretation of risk figures; Section III: Public health issues; 29: Preventing all folic acid-preventable spina bifida; 30: The half-life of cost-of-illness estimates: the case of spina bifida; 31: Insurance and coverage of care for individuals with spina bifida and other neural tube defects; 32: Assessment of health-related quality of life in individuals with neural tube defects; 33: Ethics at the forefront: moral decisions and responsibility when confronted with spina bifida

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