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颅内动脉瘤与多种先天性异常的家族性关联。

Familial association of intracranial aneurysms and multiple congenital anomalies.

作者信息

ter Berg H W, Bijlsma J B, Veiga Pires J A, Ludwig J W, van der Heiden C, Tulleken C A, Willemse J

出版信息

Arch Neurol. 1986 Jan;43(1):30-3. doi: 10.1001/archneur.1986.00520010026015.

Abstract

The familial occurrence of intracranial aneurysms and the possible relationship with connective tissue disease are discussed. We studied a large family in which seven members presented with aneurysms. Another family member presented with a subarachnoidal hemorrhage. Two other family members each presented with Marfan's syndrome and an unclassified multiple congenital anomalies syndrome, respectively. The multiplicity of the aneurysms in four members is in excess of that found in sporadic or familial cases with intracranial aneurysms. We suggest a common cause, eg, a connective tissue disorder for both the intracranial aneurysms, the Marfan's syndrome, and the unclassified syndrome.

摘要

本文讨论了颅内动脉瘤的家族性发病情况以及与结缔组织疾病的可能关系。我们研究了一个大家族,其中有七名成员患有动脉瘤。另一名家族成员出现了蛛网膜下腔出血。另外两名家族成员分别患有马凡综合征和一种未分类的多发性先天性异常综合征。四名成员的动脉瘤多发性超过了散发性或家族性颅内动脉瘤病例中的发现。我们认为颅内动脉瘤、马凡综合征和未分类综合征存在共同病因,例如结缔组织疾病。

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