Katsumi O, Tanino T, Hirose T, Larson E W, Skladzien C J
Jpn J Ophthalmol. 1985;29(3):282-9.
Four cases of Laurence-Moon-Bardet-Biedl syndrome were studied through electrophysiological and psychophysical examinations, and findings were correlated with those of fluorescein angiography. In all cases the macula showed degenerative changes, including a bull's eye appearance. The fundus periphery could be devoid of clumps of pigmentation, but all cases showed profound functional abnormalities that affected the macula and the periphery, impairing both the cone and rod systems equally. Bull's eye macula associated with severe, diffuse functional abnormality of the macula and peripheral retina, along with obesity and mental retardation, help establish the diagnosis of Laurence-Moon-Bardet-Biedl syndrome.
通过电生理和心理物理学检查对4例劳-穆-巴-比综合征患者进行了研究,并将结果与荧光素血管造影结果进行了关联。在所有病例中,黄斑均显示退行性改变,包括靶心样外观。眼底周边部可能没有色素沉着团块,但所有病例均显示出影响黄斑和周边部的严重功能异常,同等程度地损害了视锥和视杆系统。伴有黄斑和周边视网膜严重弥漫性功能异常的靶心样黄斑,以及肥胖和智力迟钝,有助于确立劳-穆-巴-比综合征的诊断。