家族性淀粉样多神经病(FAP)是一种罕见的严重淀粉样变的遗传性疾病,因经肝遗传性变异的转甲状腺蛋白引起神经部位的沉积所致的一种神经病,很少有左室收缩功能障碍,但可发生心脏传导系统的紊乱和猝死。目前还没有关于此病在心脏神经学方面的阐述,可能与交感神经的变化有关。故而 Familial amyloid polyneuropathy (FAP) is a rare, hereditary, amyloidogenic disease that results from the deposition of neurogenic sites due to transhepatic thyroid protein mutations in the liver, with few left ventricular Systolic dysfunction, but disorders and sudden cardiac death can occur. There is no statement about the disease in cardiac neurology, which may be related to the changes of sympathetic nerves. Therefore