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Osteogenesis imperfecta. Review of the literature with presentation of 29 cases.

作者信息

Shoenfeld Y

出版信息

Am J Dis Child. 1975 Jun;129(6):679-87. doi: 10.1001/archpedi.1975.02120430019007.

DOI:10.1001/archpedi.1975.02120430019007
PMID:1098447
Abstract

Twelve families with 29 patients showing various patterns of osteogenesis imperfecta are described, along with the genetic, pathological, and clinical features. No abnormal blochemical features were found. It has been shown that the best treatment is prophylactic (such as intramedullary nailingy or supportive. There was no remarkable improvement from any form of medical treatment. These data are compared to those of other authors.

摘要

相似文献

1
Osteogenesis imperfecta. Review of the literature with presentation of 29 cases.
Am J Dis Child. 1975 Jun;129(6):679-87. doi: 10.1001/archpedi.1975.02120430019007.
2
Osteogenesis imperfecta with dominant inheritance and normal sclerae.具有显性遗传和正常巩膜的成骨不全症。
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[The radiology of osteogenesis imperfecta].[成骨不全症的放射学]
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Osteogenesis imperfecta.
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Neurosurgical Implications of Osteogenesis Imperfecta in a Child after Fall: Case Illustration.一名儿童跌倒后成骨不全症的神经外科影响:病例说明
J Pediatr Neurosci. 2018 Oct-Dec;13(4):459-461. doi: 10.4103/JPN.JPN_9_18.
2
Bisphosphonate treatment in the oim mouse model alters bone modeling during growth.双膦酸盐治疗oim小鼠模型会改变生长过程中的骨塑形。
J Biomech. 2008 Dec 5;41(16):3371-6. doi: 10.1016/j.jbiomech.2008.09.028. Epub 2008 Nov 20.
3
Iliac bone histomorphometry in adults and children with osteogenesis imperfecta.
成骨不全症成人和儿童的髂骨组织形态计量学
J Clin Pathol. 1984 Oct;37(10):1081-9. doi: 10.1136/jcp.37.10.1081.
4
Osteogenic sarcoma complicating osteogenesis imperfecta tarda.成骨不全症迟发型并发骨肉瘤
Eur J Pediatr. 1978 Oct 12;129(3):215-8. doi: 10.1007/BF00442166.