常染色体显性遗传的渗出性玻璃体视网膜病变首先由Criswick等报道,为双侧性家族性进行性疾患,酷似晶体后纤维增生症,但无早产或给氧史。Gow等指出该病为常染色体显性遗传。Ober等完整地描述了其一系列表现,并强调出血和视网膜脱离是对视力的主要威胁。病变的发展限于生命的早期,18岁后不再有视力下降。 Autosomal dominant exudative vitreoretinopathy was first reported by Criswick et al. As a bilateral familial progressive disorder that resembles posterior fibroplasia without premature birth or oxygen administration. Gow pointed out that the disease is autosomal dominant. Ober et al. Fully describe a series of manifestations and emphasize that bleeding and retinal detachment are major threats to vision. The development of the lesion is limited to the early stages of life, with no loss of vision after 18 years of age.