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无症状性家族性颅内动脉瘤患病率为10%:对21个芬兰家族性颅内动脉瘤家族成员进行110次磁共振血管造影研究的初步报告

A ten percent prevalence of asymptomatic familial intracranial aneurysms: preliminary report on 110 magnetic resonance angiography studies in members of 21 Finnish familial intracranial aneurysm families.

作者信息

Ronkainen A, Hernesniemi J, Ryynänen M, Puranen M, Kuivaniemi H

机构信息

Department of Neurosurgery, University of Kuopio, Finland.

出版信息

Neurosurgery. 1994 Aug;35(2):208-12; discussion 212-3. doi: 10.1227/00006123-199408000-00005.

Abstract

The population in eastern Finland has been stable for generations, causing a high degree of genetic isolation and providing excellent possibilities for follow-up studies. Of 91 families with familial intracranial aneurysms, 21 were randomly selected for prospective magnetic resonance angiography studies for intracranial aneurysms. Sixteen intracranial aneurysms were detected in 11 asymptomatic family members of a total of 110 studied. The prevalence of intracranial aneurysms among these familial intracranial aneurysm families is 10%, approximately 10 times higher than in the average population. Our findings suggest that family members of familial intracranial aneurysm families should be examined for intracranial aneurysms. Familial intracranial aneurysm may be a genetic disorder.

摘要

芬兰东部的人口几代以来一直保持稳定,导致了高度的基因隔离,并为后续研究提供了绝佳的机会。在91个患有家族性颅内动脉瘤的家庭中,随机选择了21个家庭进行颅内动脉瘤的前瞻性磁共振血管造影研究。在总共110名接受研究的无症状家庭成员中,检测到16个颅内动脉瘤。这些家族性颅内动脉瘤家庭中颅内动脉瘤的患病率为10%,大约是普通人群的10倍。我们的研究结果表明,应该对家族性颅内动脉瘤家庭的成员进行颅内动脉瘤检查。家族性颅内动脉瘤可能是一种遗传性疾病。

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