美《医学》杂志第58卷第3期(1979年5月)第209页报道:对患有家族性嗜铬细胞瘤并发希培耳氏-林道氏病(本刊注:希培耳氏病为视网膜血管瘤病;林道氏病为中枢神经系统血管瘤病。)的一族人进行了长期流行病学和实验室研究。13名家族成员受到此综合症的影响,并且此病的特点表现为一种常染色体优式型。13名病人中,7人仅患嗜铬细胞瘤。其余6名病人中1人患嗜铬细胞瘤并有希培耳氏-林道氏病,4人仅患嗜铬细胞瘤及视网膜 Journal of the American Journal of Medicine 58(3) (May 1979), p. 209, reports on the occurrence of Familial pheochromocytoma with Heppel-Lindt’s disease. A group of people with retinal angiomatosis; Lindau’s disease with central nervous system angiomatosis. Long-term epidemiology and laboratory studies. Thirteen family members were affected by this syndrome, and the disease was characterized by an autosomal superiority type. Of the 13 patients, 7 had pheochromocytoma. One of the remaining 6 patients suffered from pheochromocytoma with Hibelle-Lindner’s disease, and only 4 had pheochromocytoma and retina