Dysplasia of C-1 and craniocervical instability in patients with Shprintzen-Goldberg syndrome -: Case report and review of the literature

被引:2
|
作者
Joedicke, Andreas
Hahn, Andreas
Berthold, Lars D.
Scharbrodt, Wolfram
Boeker, Dieter-Karsten
机构
[1] Univ Giessen, Med Ctr, Dept Neurosurg, D-35385 Giessen, Germany
[2] Univ Giessen, Med Ctr, Dept Pediat Neurol & Epileptol, D-35385 Giessen, Germany
[3] Univ Giessen, Med Ctr, Dept Pediat Radiol, D-35385 Giessen, Germany
关键词
Shprintzen-Goldberg syndrome; craniocervical instability; subaxial instability; occipitocervical fusion; pediatric neurosurgery;
D O I
10.3171/ped.2006.105.3.238
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Shprintzen-Goldberg syndrome is a rare connective tissue disorder characterized by marfanoid habitus and additional dysmorphic stigmata. Craniocervical anomalies occur in fewer than 30% of cases. Serious vertebral instability can also occur, albeit rarely. The authors report on the first patient treated with surgical fusion at the craniocervical junction because of a C-1 dysplasia and severe instability. The skeletal and cardiovascular anomalies that can pose additional problems for surgical treatment and perioperative care are discussed in detail.
引用
收藏
页码:238 / 241
页数:4
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