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结节性硬化症中结节数量和位置的预后意义

Prognostic significance of tuber count and location in tuberous sclerosis complex.

作者信息

Doherty Colin, Goh Suzanne, Young Poussaint Tina, Erdag Namik, Thiele Elizabeth A

机构信息

Department of Neurology, Massachusetts General Hospital, 55 Fruit Street, VBK 830, Boston, 02114-3117, USA.

出版信息

J Child Neurol. 2005 Oct;20(10):837-41. doi: 10.1177/08830738050200101301.

Abstract

The objectives of this study were (1) to test the utility of tuber count and tuber location as biomarkers of disease severity in patients with tuberous sclerosis complex and (2) to examine the relationship between gene mutation, tuber count, and tuber location. We found that an increased tuber count per lobe and in total was associated with an increased risk of infantile spasms (P < .01). Increased tuber count in the occipital lobe was associated with an increased risk of pervasive developmental disorder (P = .0074). The mean tuber count per lobe and in total was higher in those with poorly controlled seizures and those with off-track development; however, these differences were not statistically significant (P > .01). The TSC2 gene mutation was associated with a significant increase in the tuber count per lobe and in total (P < .01). In summary, increased tuber count is strongly associated with infantile spasms and a TSC2 gene mutation. Seizure control and developmental delay do not show the strong association with tuber count suggested by the earlier literature.

摘要

本研究的目的是

(1)测试结节计数和结节位置作为结节性硬化症患者疾病严重程度生物标志物的效用;(2)研究基因突变、结节计数和结节位置之间的关系。我们发现,每叶和总的结节计数增加与婴儿痉挛风险增加相关(P <.01)。枕叶结节计数增加与广泛性发育障碍风险增加相关(P =.0074)。癫痫发作控制不佳和发育偏离的患者每叶和总的平均结节计数更高;然而,这些差异无统计学意义(P >.01)。TSC2基因突变与每叶和总的结节计数显著增加相关(P <.01)。总之,结节计数增加与婴儿痉挛和TSC2基因突变密切相关。癫痫发作控制和发育迟缓与早期文献所提示的结节计数没有强烈关联。

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