Godel V, Nemet P, Lazar M
Doc Ophthalmol. 1981 Jul 15;51(3):277-88. doi: 10.1007/BF00143890.
Retinal dysplasia is defined as an abnormal growth and differentiation of embryonic retina being more a secondary lesion rather than a disease. Clinically, the disorder may present itself in a surprisingly wide range of severity or of degree from retinal folds to vascularized masses in the vitreous cavity. The condition may appear monosymptomatically, involving only the eye, or as complex disorders with multisystemic anomalies. The histopathologic findings in this disorder recognize characteristic structural deviations of the retina and the pathogenesis seems to be related to the lack of the normal histogenesis of the pigment epithelium. Impaired genetic mechanisms seem to contribute to the etiology of some forms of retinal dysplasia.
视网膜发育异常被定义为胚胎视网膜的异常生长和分化,更多的是一种继发性病变而非一种疾病。临床上,该病症的严重程度或程度范围惊人地广泛,从视网膜褶皱到玻璃体腔中的血管化肿块。这种情况可能单症状出现,仅累及眼睛,也可能作为伴有多系统异常的复杂病症出现。该病症的组织病理学发现识别出视网膜的特征性结构偏差,其发病机制似乎与色素上皮正常组织发生的缺乏有关。受损的遗传机制似乎促成了某些形式的视网膜发育异常的病因。