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Author: Daniel Bergsma
Publisher:
ISBN: 9780333278765
Category : Abnormalities, Human
Languages : en
Pages : 1183
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Book Description
Author: Daniel Bergsma
Publisher:
ISBN: 9780333278765
Category : Abnormalities, Human
Languages : en
Pages : 1183
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Book Description
Author: Daniel Bergsma
Publisher:
ISBN:
Category : Abnormalities, Human
Languages : en
Pages : 1076
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Book Description
842 presently recognized birth defect syndromes are described in the Compendium, and 641 photographs of defects are presented in the Atlas. Separate tables of contents appear in English, French, German, and Spanish. Tables. Author index, extensive subject index.
Author: Daniel Bergsma
Publisher:
ISBN:
Category :
Languages : en
Pages : 1006
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Book Description
Author: Daniel Bergsma
Publisher: Springer
ISBN: 1349051314
Category : Medical
Languages : en
Pages : 1214
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Book Description
Author: T.V.N. Persaud
Publisher: Springer Science & Business Media
ISBN: 9401166218
Category : Medical
Languages : en
Pages : 395
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Book Description
Surprisingly, the beginning of a modern approach This collection of articles and commentaries is an to the problems of birth defects is relatively recent integration of information from many disciplines, and dates from Gregg's classical report in 1941 that and presents a comprehensive survey of both recent mothers who contracted rubella during the first tri and previously reported work related to the major mester of pregnancy gave birth to infants with severe aspects of birth defects. In particular, an attempt multiple anomalies. For the first time, an environ has been made to provide a critical assessment of mental agent was found to be teratogenic in man current concepts and to identify areas in need of and was documented in a thoroughly convincing further investigation. manner. Since then, many important discoveries The scope of this volume and space limitations and significant developments have been made, par precluded discussion of and reference to all papers ticularly in the areas of environmental teratogenesis, of relevance or importance: a work of the present hereditary mechanisms, and prenatal diagnosis. nature must necessarily be selective. Some good In recent years, there has been an impressive papers have been left out or given relatively little surge of interest in the causes and prevention of consideration. It is my hope that the list of Further birth defects. Undoubtedly this resulted not only References will be consulted and should compensate from the thalidomide tragedy, but also from the for this lack of completeness.
Author: American Academy of Pediatrics
Publisher:
ISBN:
Category : Abnormalities, Human
Languages : en
Pages : 134
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Book Description
Author: Robin M. Winter
Publisher: Springer
ISBN: 1489931090
Category : Medical
Languages : en
Pages : 1441
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Book Description
The size of the problem, can be assessed This book is an off-shoot of the computerized from the following. Of 50 children bom, 1 London Dysmorphology Database which is now widely used by many geneticists and will have an easily detectable major malfor mation. Many of these will have a single dysmorphologists. Both the database and this malformation, but in the region of 8 in 1000 book have arisen out of a need to cope with the ever increasing nurober of multiple will have multiple abnormalities. This group will include 50% with chromosomal disorders congenital anomaly syndromes, especially recognizable by performing a karyotype, the details about their features and where infor mation can be found in the Iiterature. Indeed rest needing tobe diagnosed by other means. there are more than 2000 non-chromosomal It is to the diagnosis of this latter group that this book is dedicated. multiple malformation syndromes to which access is essential. If computerized databases have solved THE DIAGNOSIS OF DYSMORPHIC some of the problems, why is there a need SYNDROMES for this book? There are many physicians who do not have a desk computer or do not History feel at ease in using one. In addition geneticists are doing more satellite clinics and Before identifying the specific dysmorphic in some circumstances it would be more features, at least a three generation family history needs to be taken. It is necessary to convenient to carry a book than a computer.
Author: T.V.N. Persaud
Publisher: Springer Science & Business Media
ISBN: 9401166692
Category : Science
Languages : en
Pages : 257
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Book Description
Birth defects have assumed an importance even greater now than in the past because infant mortality rates attributed to congenital anomalies have declined far less than those for other causes of death, such as infectious and nutritional diseases. As many as 50 % of all pregnancies terminate as miscarriages, and in the majority of cases this is the result of faulty intrauterine development. Major congenital malformations are present in at least 2 % of all liveborn infants, and 22 % of all stillbirths and infant deaths are associated with severe congenital anomalies. Not surprisingly, there has been a great proliferation of research into the problems of developmental abnormalities over the past few decades. This series, Advances in the Study of Birth Defects, was conceived in order to provide a comprehensive focal source of up-to-date information for physi cians concerned with the health of the unborn child and for research workers in the fields of fetal medicine and birth defects. The first four volumes featured recent experimental work on selected areas of high priority and intensive investigation, including mechanisms of teratogenesis, teratological evaluation, molecular and cellular aspects of abnormal development, and neural and behavioural teratology. It seems logical and timely that the clinical aspects should now be presented. Accordingly, leading experts were invited to review a broad range of common problems from the standpoint of embryology, aetiology, clinical manifestations, diagnosis and management. This volume deals with genetic disorders and prenatal diagnosis.
Author: World Health Organization
Publisher: World Health Organization
ISBN: 9241549289
Category : Medical
Languages : en
Pages : 162
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Book Description
The goal of this course is to provide participants with the foundational skills needed to begin the development implementation and ongoing improvement of a congenital anomalies surveillance programme in particular for countries with limited resources. It focuses on the methodology needed to develop either population-based or hospitalbased surveillance programmes. A set of congenital anomalies will be used as examples throughout this course. The specific examples used are typically severe enough that they would probably be captured within the first few days after birth have a significant public health impact and for some of them have the potential for primary prevention. Target audience This course is designed for individuals who are directly involved in the development implementation and daily activities related to congenital anomalies surveillance programmes in their countries and who will directly teach others. Learning objectives By the end of this course participants will be able to: 1. describe how to use data for the development of prevention campaigns and policy/programme evaluation; 2. describe how to best present data to policy-makers; 3. identify selected major external congenital anomalies for monitoring; 4. describe the tools needed to ascertain and code congenital anomalies; 5. describe the processes for managing and analysing data; 6. demonstrate how to calculate the birth prevalence of congenital anomalies.
Author:
Publisher:
ISBN:
Category : Medicine
Languages : en
Pages : 1368
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Book Description
