Larsen P D, Hellbusch L C, Lefkowitz D M, Schaefer G B
Department of Neurology, Creighton University Medical Center, Omaha, Nebraska 68131, USA.
Pediatr Neurol. 1997 Jul;17(1):74-6. doi: 10.1016/s0887-8994(97)00007-6.
We report a kindred with cerebral arteriovenous malformations in three generations, suggesting autosomal dominant inheritance in this family. Screening asymptomatic persons with a family history for cerebral arteriovenous malformations is discussed.
我们报告了一个三代人中患有脑动静脉畸形的家族,提示该家族中存在常染色体显性遗传。本文讨论了对有脑动静脉畸形家族史的无症状个体进行筛查的问题。