Robitaille J M, Monsein L, Traboulsi E I
Johns Hopkins Center for Hereditary Eye Diseases, Wilmer Opthalmological Institute, Baltimore, MD, USA.
Ophthalmic Genet. 1996 Dec;17(4):215-8. doi: 10.3109/13816819609057896.
Primary retinal telangiectasis or Coats' disease is a non-hereditary retinal vascular abnormality consisting of incompetent telangiectatic and aneurysmal retinal vessels. It is characteristically found unilaterally in boys and occasionally may be associated with other systemic disorders. The authors report the first case of primary retinal telangiectasis with a concomitant diffuse central nervous system venous abnormality.
原发性视网膜毛细血管扩张症或科茨病是一种非遗传性视网膜血管异常，由功能不全的毛细血管扩张性和动脉瘤性视网膜血管组成。其特征是在男孩中单侧发病，偶尔可能与其他全身性疾病有关。作者报告了首例伴有弥漫性中枢神经系统静脉异常的原发性视网膜毛细血管扩张症病例。
