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畸形综合征。脊椎发育不全、关节挛缩和腘窝翼状胬肉。

Malformation complex. Spondylohypoplasia, arthrogryposis, and popliteal pterygium.

作者信息

Turkel S B, Iseri A L, Fujimoto A O

出版信息

Am J Dis Child. 1980 Jan;134(1):42-5.

PMID:7350786
Abstract

Two unrelated children were born with severe congenital malformations: a girl now seven years old and a boy who died in the newborn period. Both had severe cervical hyperextension, severe flexion deformities of the limbs, and bilateral popliteal pterygia. Postmortem examination of the second case showed small, well-formed thoracic vertebrae with mild epidural fibrosis and hemorrhage. These births defects are rare and usually occur separately. We postulate that they are related in these two cases; that the arthrogryposis and popliteal pterygia were probably the result of the spondylohypoplasia and associated changes; and that together, these related defects may constitute a new malformation complex.

摘要

两名无血缘关系的儿童出生时患有严重先天性畸形

一名七岁女孩,另一名男婴在新生儿期死亡。两人均有严重的颈椎过度伸展、四肢严重屈曲畸形以及双侧腘窝翼状胬肉。第二例尸检显示胸椎小且形态良好,伴有轻度硬膜外纤维化和出血。这些出生缺陷很罕见,通常单独出现。我们推测在这两例中它们有关联;关节挛缩和腘窝翼状胬肉可能是脊椎发育不全及相关变化的结果;并且这些相关缺陷可能共同构成一种新的畸形综合征。

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Spondylohypoplasia, arthrogryposis, and popliteal pterygium.脊椎发育不全、关节挛缩和腘窝翼状胬肉。
Am J Dis Child. 1980 Oct;134(10):1001. doi: 10.1001/archpedi.1980.02130220077034.
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