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成骨不全症 V 型患儿第一年干骺端的放射学表现演变:发病机制的线索。

Evolution of the radiographic appearance of the metaphyses over the first year of life in type V osteogenesis imperfecta: clues to pathogenesis.

机构信息

Academic Unit of Child Health, University of Sheffield, and Sheffield Children's Hospital NHS Foundation Trust, Sheffield, United Kingdom.

出版信息

J Bone Miner Res. 2011 Apr;26(4):894-8. doi: 10.1002/jbmr.258.

Abstract

We present the first report of the development of characteristic radiologic appearances of long bones during the first year of life in an infant with type V osteogenesis imperfecta (OI). We show the evolution of metaphyseal abnormalities from a rickets-like appearance to the classically described dense metaphyseal bands. These abnormalities suggest that the underlying defect in type V OI may involve a molecule common to both bone and cartilage that is involved in the regulation of growth plate development and metadiaphyseal ossification. Our findings provide new insights into skeletal development in type V OI and potentially yield useful clues to the identity of the defect underpinning the condition.

摘要

我们首次报道了一例 V 型成骨不全症(OI)婴儿在生命第一年长骨的特征性放射学表现。我们展示了干骺端异常从佝偻病样外观到经典描述的致密干骺端带的演变。这些异常表明,V 型 OI 的潜在缺陷可能涉及一种同时存在于骨骼和软骨中的分子,该分子参与生长板发育和骨干骺端骨化的调节。我们的发现为 V 型 OI 的骨骼发育提供了新的见解,并可能为该疾病潜在缺陷的鉴定提供有用线索。

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