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Titlebook: Orthopaedic Problems in Inherited Skeletal Disorders; Frank Horan,Peter Beighton Book 1982 Springer-Verlag Berlin Heidelberg 1982 Erbkrank

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發(fā)表于 2025-3-21 16:55:20 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Orthopaedic Problems in Inherited Skeletal Disorders
編輯Frank Horan,Peter Beighton
視頻videohttp://file.papertrans.cn/705/704730/704730.mp4
圖書封面Titlebook: Orthopaedic Problems in Inherited Skeletal Disorders; Frank Horan,Peter Beighton Book 1982 Springer-Verlag Berlin Heidelberg 1982 Erbkrank
描述Inherited skeletal disorders have a fascination for many medical and surgical disciplines. For the geneticist there is interest in the study of families and their inheritance of lesions. The paediatrician is concerned because most of the disorders present in childhood as a problem in clinical differential diagnosis. The radiologist is interested because of the manifest, multiple and curious bone changes that provide a challenge in diagnosis and classification. The orthopaedic surgeon is involved because they present a challenge in the management of the many and various lesions of the limbs and trunk. Most of the text books are slanted towards one or other aspect of the subject, depending upon the specialist interests of their author. Though informative to colleagues in their own discipline, the information which they contain is liable to be overwhelming in its complexity or unhelpful in its content for the orthopaedic surgeon or trainee. Frank Horan and Peter Beighton have aimed their admirable and concise monograph to help the orthopaedic surgeon-the one individual who is likely to be able to ameliorate the musculo-skeletal problems from which so many of the children and adults wi
出版日期Book 1982
關(guān)鍵詞Erbkrankheit; Orthop?die; Osteogenesis imperfecta; bone; cartilage; childhood; chromosome; classification; c
版次1
doihttps://doi.org/10.1007/978-1-4471-1326-3
isbn_softcover978-1-4471-1328-7
isbn_ebook978-1-4471-1326-3
copyrightSpringer-Verlag Berlin Heidelberg 1982
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Mucopolysaccharidoses (MPS) and Other Storage Disorders, activity of any of these may cause a block in the breakdown process with an accumulation of the semi-degraded compound within the cell. The disorders are classified according to the type of substance which accumulates, hence the designation mucopolysaccharidoses, sphingolipidoses, and gangliosidoses.
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Nomenclature and Terminology,nto specific disorders. The realisation that the recognition and accurate definition of individual abnormalities facilitates satisfactory management and prognostication, has led to increased efforts towards the separation and precise identification of individual syndromes.
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Mucopolysaccharidoses (MPS) and Other Storage Disorders,ith intracellular degradation of macromolecular compounds into smaller component units. This process is dependent upon specific enzymes, and defective activity of any of these may cause a block in the breakdown process with an accumulation of the semi-degraded compound within the cell. The disorders
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Frank Horan MSc, FRCS,Peter Beighton MD, PhD, FRCP, DCHn lithic functional analysis. These sources inform about the use of certain tools, operative chains and full technical processes, or about the different contexts in which production is carried out. Thus, we can obtain insights on the use and management of tools, production objectives, product manage
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Frank Horan MSc, FRCS,Peter Beighton MD, PhD, FRCP, DCHal variation in response to treatment. These features make RA an ideal condition to develop biomarkers for its preclinical detection, diagnosis, subtyping, prognostic stratification, and selection of most optimal treatment. While a number of markers have been assessed for their biomarker quality, cu
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