A Case Report of a Cervical Exostosis and Spinal Cord Compression in a Child with Trichorhinophalangeal Syndrome II

被引：0

作者：

Farook, Shahme ^{[1
]}

Mistry, Aekta ^{[2
]}

Hussain, Muniba ^{[2
]}

Crimmins, Darach ^{[3
]}

机构：

[1] Univ Coll London Hosp, Dept Head & Neck Surg, 235 Euston Rd, London NW1 2BU, England

[2] Northwick Pk Hosp & Clin Res Ctr, Dept Oral & Maxillofacial Surg, London, England

[3] Childrens Univ Hosp, Dept Neurosurg, Dublin, Ireland

来源：

JOURNAL OF PEDIATRIC NEURORADIOLOGY | 2015年 / 4卷 / 02期

关键词：

trichorhinophal-angeal syndrome; Langer-Giedion syndrome; hereditary multiple exostoses; spinal cord compression; cervical exostosis;

D O I：

10.1055/s-0036-1579623

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

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.

引用

页码：41 / 44

页数：4

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