cerebral cavernous malformation ccm 脑海绵状血管瘤
cavernous venous malformation 海绵状静脉畸形
cavernous vascular malformation 海绵状血管畸形
Objective To detect the mutations of Krit-1 gene that cause familial cerebral cavernous malformation (CCM) in the Han ethnic origin.
目的探查汉族家族性中枢神经系统海绵状血管畸形(CCM)的突变基因。
Conclusion When the patients with brainstem cavernous malformation exhibited progressive neural function deficits and mass effect, it should be considered as good candidates for surgical therapy.
结论 脑干海绵状血管瘤表现为进行性神经功能缺失、具有占位效应、接近脑干表面者可考虑手术治疗;
Purpose To probe the pathogenesis of cavernous venous malformation by observing its pathologic structure.
目的观察体表海绵状静脉畸形的病理结构,探讨其畸形的病理机制。
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