Erikson A, Wahlberg I
Acta Ophthalmol (Copenh). 1985 Apr;63(2):221-5. doi: 10.1111/j.1755-3768.1985.tb01537.x.
Ocular abnormalities in 22 patients with the Norrbottnian type of Gaucher disease are reported. During their first 10 years of life 10 patients had a horizontal gaze abnormality simulating congenital ocular motor apraxia. Examination showed signs of supranuclear oculomotor disturbances in several of them. Thirteen patients had squint secondary to weakness of the abductor muscles; 8/21 examined patients exhibited white retinal infiltrates, which mostly appeared after splenectomy; 8/19 examined patients had myopia. Except for the retinal changes, no connection was found between the abnormalities and the severity of the disease.
报告了22例诺尔伯顿型戈谢病患者的眼部异常情况。在他们生命的最初10年里,10例患者存在水平注视异常,类似先天性眼球运动失用症。检查发现其中几例有核上性眼球运动障碍的体征。13例患者因外展肌无力继发斜视;在21例接受检查的患者中,8例出现视网膜白色浸润,大多在脾切除术后出现;在19例接受检查的患者中,8例有近视。除视网膜改变外,未发现这些异常与疾病严重程度之间存在关联。