Wilson W A
Calif Med. 1969 Dec;111(6):446-9.
Changes in ocular findings have been noted in association with several metabolic diseases. In homocystinuria the crystalline lens in the majority of cases is subluxated inferiorly, while in Marfan's syndrome the dislocation was upward. In cystinosis, slit-lamp examination reveals numerous gold crystal-like cystine deposits in both the cornea and bulbar conjunctiva. Patients with galactosemia have cataracts of the "oil drop" type, which usually can be seen with an ophthalmoscope even though the opacity is not dense. Eight patients with Lowe's syndrome who were observed had cataracts, and four of them had severe glaucoma. Three of five patients with glycogen storage disease Type I had yellowish deposits in the macular and paramacular areas, thought to be due to hypercholesterolemia.
已注意到眼部表现的变化与多种代谢性疾病有关。在同型胱氨酸尿症中,大多数病例的晶状体向下半脱位,而在马凡综合征中,脱位向上。在胱氨酸病中,裂隙灯检查可发现角膜和球结膜有许多金晶体样的胱氨酸沉积。半乳糖血症患者有“油滴”型白内障,即使混浊不严重,通常用检眼镜也能看到。观察到的8例 Lowe 综合征患者有白内障,其中4例有严重青光眼。5例I型糖原贮积病患者中有3例在黄斑和黄斑旁区域有黄色沉积物,认为是高胆固醇血症所致。