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Titlebook: Clinical Embryology; An Atlas of Congenit Robert Carachi,Sameh Helmi Edward Doss Book 2019 Springer International Publishing AG, part of Sp

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发表于 2025-3-21 18:03:50 | 显示全部楼层 |阅读模式
书目名称Clinical Embryology
副标题An Atlas of Congenit
编辑Robert Carachi,Sameh Helmi Edward Doss
视频video
概述Combines information on embryological development with detailed presentation of congenital malformations.Explains how congenital malformations develop.Includes a wealth of illustrations, most of them
图书封面Titlebook: Clinical Embryology; An Atlas of Congenit Robert Carachi,Sameh Helmi Edward Doss Book 2019 Springer International Publishing AG, part of Sp
描述This comprehensive atlas is unique in combining information on the embryological development of the human with detailed presentation of the congenital malformations encountered in clinical practice. As a consequence it will not only assist practitioners and trainees in recognizing and evaluating malformations, but also enable them to understand how a malformation has developed and to explain the mystery of congenital malformations to relatives and patients. The book is organized according to anatomic region, with additional chapters on hernias, tumors, lymphogenesis and lymphatic malformations. According to WHO statistics, each year congenital anomalies result in approximately 3.2 million birth defect-related disabilities worldwide. All too often, however, training in embryology is now a neglected area, and medical graduates frequently lack confidence in their knowledge of the field. Clinical Embryology: An Atlas of Congenital Malformations will help to rectify this deficit and toensure that malformations are comprehended and managed appropriately. It will be of value for postgraduate trainees in pediatric surgery, pediatrics, and neonatology, undergraduate medical students, and ge
出版日期Book 2019
关键词Birth defect; Deformity; Disability; Neonatology; Ontogeny
版次1
doihttps://doi.org/10.1007/978-3-319-26158-4
isbn_ebook978-3-319-26158-4
copyrightSpringer International Publishing AG, part of Springer Nature 2019
The information of publication is updating

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发表于 2025-3-21 22:03:42 | 显示全部楼层
A. M. Hirsch,M. R. Lum,N. A. Fujishigef causing birth defects following exposure during pregnancy. Substances with teratogenic qualities include drugs, environmental agents, infections, toxins and nutrients. The probability of a malformation being produced depends on the dose of the agent, the stage at which the embryo is exposed and th
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Genetics of Root Hair Formation,ingle fertilized cell, the ., undergoes sequential cell divisions followed by coordinated cell proliferation, migration and differentiation, to create something as intricately complex as a human foetus [1]. Interestingly, the various stages of the human embryonic development (see Table 6.1) share ho
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Alison Cavell,Claire S. Griersonal malformations. He/she is a part of the prenatal team and parents should always be referred to him/her when a surgical malformation is suspected, even when termination of pregnancy is planned because of an expected poor prognosis.
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https://doi.org/10.1007/978-0-387-92765-7 severe deformity and are a challenge to all who work with them. Their origin is felt to be at the junction of facial processes and the clefts, often centre around the oral cavity and connect with the nose, eye, maxilla, ear and cranial vault – however, are often partial or incomplete. They are comp
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Improving Safety of Cassava Productsformations of the TMJ and mandible which by their very nature are often associated with a syndrome. The most commonly encountered malformations of this region will be discussed individually, to include the more commonly known and documented syndromes.
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https://doi.org/10.1007/978-3-030-92022-7overall prevalence of craniosynostosis has been estimated at between 1 in 2100 and 1 in 2500 live births. It is most often an isolated finding, affecting the sagittal or coronal sutures, but can also occur as part of a syndrome, with additional findings such as limb abnormalities and developmental d
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Transforming Yam Seed Systems in West Africaanchial apparatus, whereas the inner ear develops separately from the otic placode. Deviations from the normal pattern of embryogenesis at varying stages of development can give rise to a wide variety of congenital malformations. Because of how closely these structures are linked, a malformation aff
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