首页> 外文期刊>Journal of pediatric neuroradiology. >A Case Report of a Cervical Exostosis and Spinal Cord Compression in a Child with Trichorhinophalangeal Syndrome II
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A Case Report of a Cervical Exostosis and Spinal Cord Compression in a Child with Trichorhinophalangeal Syndrome II

机译:腹腔膜综合征II的儿童宫颈失明和脊髓压缩的病例报告

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摘要

Trichorhinophalangeal syndrome (TRPS) is an extremely rare complex genetic disorder with autosomal dominant inheritance. This case report discusses the management of a 4-year-old child with TRPS II (previously known as Langer-Giedion syndrome), who presented with right-sided hemiparesis and a limping gait secondary to spinal cord compression at the level of C1. Here, we document a child who underwent a successful decompressive laminectomy, highlighting the importance of a multidisciplinary team approach in managing rare and complex cases.
机译:Trichorhinophalangeal综合征(TRP)是一种极其罕见的复杂性遗传障碍,具有常染色体显性遗传。 本案报告讨论了4岁儿童的TRP II(以前称为Langer-Giedion综合征)的管理,他呈现出右侧血管血清和跛行的静脉曲张,在C1的水平下进行脊髓压缩。 在这里,我们向一个接受成功的减压叠层切除术的儿童记录了一个经历了成功的压缩叠层,突出了多学科团队方法在管理稀有和复杂案件方面的重要性。

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