Osteogenesis Imperfecta Associated with Ehlers‐Danlos Syndrome
Osteogenesis Imperfecta Associated with Ehlers‐Danlos Syndrome
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与埃勒斯-当洛斯综合征相关的成骨不全
DOI：
10.1111/j.1651-2227.1955.tb04140.x
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发表时间：
1955
期刊：
影响因子：
--
通讯作者：
T. Iversen
中科院分区：
文献类型：
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作者：
Axel Biering;T. Iversen
在同一患者中合并成骨不全和埃勒斯-丹洛斯综合征似乎以前没有报道过。Kanof(15)描述了一位患有Ehler-Danlos综合征、蓝巩膜和骨质疏松的患者，但没有骨折。在Johnson和Falls关于Ehler-Danlos综合征的论文(14)之后的讨论中，Johnson说：“在成骨不全(骨碎性骨质疏松症)中，人们也可能发现关节的高度伸展性。蓝色巩膜和反复骨折史应该有助于将这种情况与Ehler-Dan-10s综合征相鉴别。这些变化将在未来的埃勒斯-丹洛斯综合征病例中寻找。“
The combination of osteogenesis imperfecta and the Ehlers‐Danlos syndrome in the same patient does not seem to have been reported before. Kanof (15) described a patient with Ehlers‐Danlos syndrome, blue sclerae and osteoporosis, but without fractures. In the discussion following Johnson and Falls' paper on Ehlers‐Danlos syndrome (14), Johnson said: “In osteogenesis imperfecta (fragilitas ossium) one may also find hyperextensibility of the joints. The blue scleras and history of repeated fractures should help one to differentiate this condition from the Ehlers‐Dan‐10s syndrome. These changes will be looked for in future cases of the Ehlers‐Danlos syndrome.”