Akutsu Hiroyoshi, Sonobe Makoto, Sugita Kyoichi, Nakai Yasunobu, Matsumura Akira
Department of Neurosurgery, Mito National Hospital, Mito, Ibaraki, Japan.
Neurol Med Chir (Tokyo). 2003 Sep;43(9):435-8. doi: 10.2176/nmc.43.435.
Four patients presented with familial intracranial aneurysms and familial moyamoya disease, including one patient with both familial intracranial aneurysm and moyamoya disease. Basilar bifurcation aneurysms were present in two patients, moyamoya disease in one, and both basilar bifurcation aneurysm and moyamoya disease in one. These events are most likely to arise from different genetic abnormalities associated with basilar bifurcation aneurysm and moyamoya disease.
4例患者患有家族性颅内动脉瘤和家族性烟雾病，其中1例同时患有家族性颅内动脉瘤和烟雾病。2例患者存在基底动脉分叉处动脉瘤，1例患有烟雾病，1例同时患有基底动脉分叉处动脉瘤和烟雾病。这些情况很可能源于与基底动脉分叉处动脉瘤和烟雾病相关的不同基因异常。
