首页> 外文期刊>American journal of medical genetics, Part A >Dural ectasia in children with Marfan syndrome: a prospective, multicenter, patient-control study.
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Dural ectasia in children with Marfan syndrome: a prospective, multicenter, patient-control study.

机译:马凡综合征儿童的硬脑膜扩张:一项前瞻性,多中心,患者对照研究。

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The clinical diagnosis of Marfan syndrome in childhood is difficult, because symptoms may not have developed to their full expression until adulthood. The Ghent nosology for the diagnosis of Marfan syndrome classifies dural ectasia as a major diagnostic criterion. More than two thirds of adult patients with Marfan syndrome show dural ectasia, while the frequency in childhood is unknown. This prospective multicenter observational patient-control study was performed to identify pathologic changes of the lumbosacral spine in young patients with Marfan syndrome. Design: Prospective clinical trial, multicentric, cross-sectional. Setting: MRI of the lumbosacral spine. Patients: Twenty patients with proven Marfan syndrome, 20 patients suspicious for Marfan syndrome and 38 healthy controls. Outcome measures: Vertebral body diameter (VBD) from L1 to S1, dural sac diameter (DSD) from L1 to S1, dural sac ratio (DSR), qualitative assessment of the lumbosacral spine. Results: DSD and VBD in different age groups were higher in patients with proven or suspected Marfan syndrome than in healthy controls (DSD: L1, 6-8 years, P < 0.05). VBD related to body height showed a similar growth related increase in patients with proven or suspected Marfan syndrome and controls. DSD related to body height was elevated in patients with proven or suspected Marfan syndrome at different levels of the lumbar spine. DSD at levels L1, L5, and S1, and DSR at levels L5 and S1 of patients with proven Marfan syndrome were significantly higher (P < 0.05) than in controls. Conclusion: Even during childhood pathologic changes inside the lumbosacral spine of patients with Marfan syndrome can be observed. Dural ectasia, which occurs at different levels of the lumbar spine, can be detected at levels L5 and S1 in up to 40% of patients with Marfan syndrome.
机译:儿童时期的Marfan综合征的临床诊断很困难,因为直到成年后症状才可能发展到完全表现出来。诊断马凡氏综合症的根特(Ghent)病学将硬脑膜扩张作为主要诊断标准。超过三分之二的马凡氏综合征成年患者表现出硬脑膜扩张,而儿童时期的发生频率尚不清楚。这项前瞻性多中心观察性患者对照研究旨在确定年轻Marfan综合征患者腰s部脊柱的病理变化。设计:前瞻性临床试验,多中心,横断面。地点:腰s部MRI。患者:20名证实患有马凡氏综合症的患者,20名怀疑马凡氏综合症的患者和38名健康对照者。结果测量:从L1到S1的椎体直径(VBD),从L1到S1的硬膜囊直径(DSD),硬膜囊比(DSR),腰s脊柱的定性评估。结果:证实或怀疑患有马凡氏综合征的患者在不同年龄组的DSD和VBD高于健康对照组(DSD:L1,6-8岁,P <0.05)。与身高有关的VBD在已证实或怀疑有马凡综合症和对照的患者中显示出与生长相关的相似增长。在腰椎不同水平上已证实或怀疑患有马凡综合症的患者中,与身高相关的DSD升高。经证实的马凡综合症患者的L1,L5和S1水平的DSD以及L5和S1水平的DSR显着高于对照组(P <0.05)。结论:即使在儿童期,Marfan综合征患者的腰inside骨内部也会出现病理变化。在多达40%的马凡氏综合症患者中,可以在L5和S1水平检测到发生在腰椎不同水平的硬脑膜扩张。

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