Arbisser A I, Murphree A L, Garcia C A, Howell R R
Am J Ophthalmol. 1976 Sep;82(3):465-71. doi: 10.1016/0002-9394(76)90496-7.
Three patients with typical features of mannosidosis and deficiency of alpha-mannosidase activity, who were examined ophthalmologically, had similar lenticular opacities. Corneal opacities were absent. Chamber angle and striking ophthalmoscopic anomalies occurred in two young patients who had normal electroretinograms. Two patients had strabismus. Conjunctival biopsy specimens morphologically confirmed the lysosomal nature of this disorder.
三名患有典型甘露糖苷贮积症且α-甘露糖苷酶活性缺乏的患者接受了眼科检查,他们有相似的晶状体混浊。角膜混浊不存在。两名视网膜电图正常的年轻患者出现了房角和显著的眼底异常。两名患者有斜视。结膜活检标本在形态学上证实了该疾病的溶酶体性质。