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Titlebook: Sclerosing Bone Dysplasias; Peter Beighton,Bryan J. Cremin Book 1980 Springer-Verlag Berlin Heidelberg 1980 Bone.Dysplasias.Knochendysplas

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發(fā)表于 2025-3-21 18:49:53 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Sclerosing Bone Dysplasias
編輯Peter Beighton,Bryan J. Cremin
視頻videohttp://file.papertrans.cn/863/862845/862845.mp4
圖書封面Titlebook: Sclerosing Bone Dysplasias;  Peter Beighton,Bryan J. Cremin Book 1980 Springer-Verlag Berlin Heidelberg 1980 Bone.Dysplasias.Knochendysplas
描述Much confusion exists in the accurate identification and classification of the many disorders in infancy which affect the skeleton by producing sclerosing lesions throughout the entire skeleton or in selected areas. A scholarly effort to bring order into this confusing field must be welcomed. Professors Beighton and Cremin have skillfully defined the problem and concisely yet thoroughly have identified the various sclerosing dysplasias. They bring to this task a wealth of clinical experience in their many years in the Departments of Radiology at the University of Cape Town Medical School and the Groote Schuur and Red Cross Children‘s Hospitals in Cape Town, South Africa. The authors also have had available data from the University of Cape Town Skeletal Dysplasia Registry. Professors Beighton and Cremin have used as a basis for their treatise the Paris Nomenclature (the modified version of 1977). This monograph is a felicitous combination of a working atlas and a scholarly exposition of the various sclerosing bone dysplasias, considering in detail eighteen major entities adopted from the Paris classification. Other disorders which present with osteosclerosis are also described. Thes
出版日期Book 1980
關(guān)鍵詞Bone; Dysplasias; Knochendysplasie; Knochensklerose; R?ntgendiagnostik; classification; radiology; conserva
版次1
doihttps://doi.org/10.1007/978-1-4471-1292-1
isbn_softcover978-1-4471-1294-5
isbn_ebook978-1-4471-1292-1
copyrightSpringer-Verlag Berlin Heidelberg 1980
The information of publication is updating

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沙發(fā)
發(fā)表于 2025-3-21 21:58:42 | 只看該作者
https://doi.org/10.1007/978-1-4471-1292-1Bone; Dysplasias; Knochendysplasie; Knochensklerose; R?ntgendiagnostik; classification; radiology; conserva
板凳
發(fā)表于 2025-3-22 04:10:45 | 只看該作者
Clinical and Genetic Aspects,The sclerosing bone dysplasias are all uncommon and some are distinctly rare. In order to give a perspective of their relative prevalence, the approximate totals of reported cases in the world literature and their modes of inheritance are given in Table 2–1.
地板
發(fā)表于 2025-3-22 07:52:46 | 只看該作者
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發(fā)表于 2025-3-22 11:17:33 | 只看該作者
Craniodiaphyseal Dysplasia,. et al. (1958) reported a patient with severe sclerosis of the skull, cited a similar case from . (1949), and termed the disorder ‘dysplasie craniodiaphysaire progressive.’ At this time the condition was thought to be related to .-. disease.
6#
發(fā)表于 2025-3-22 14:03:41 | 只看該作者
Sclerosteosis,Sclerosteosis was first recognised as a distinct entity when . (1958) described two unrelated South African girls with ‘osteopetrosis with syndactyly; a morphological variant of Albers-Sch?nberg disease.’ Subsequently, . (1967) used the term ‘sklerosteose,’ which in its anglicised form ‘sclerosteosis’ has gained general acceptance.
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發(fā)表于 2025-3-22 17:50:29 | 只看該作者
Diaphyseal Dysplasia (Camurati-Engelmann Disease),. (1922) described a seven-year-old boy with painful lower limbs and diaphyseal cortical thickening in the long bones of the legs. The 55-year-old father and eight of their family members in four generations were thought to be affected, and the condition was termed ‘hereditary symmetrical osteitis’.
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