Volume 3,Issue 4
Fall 2025
T188K基因引发视觉症状克雅病1例及文献复习
目的 提高临床医生对于以视觉症状起病的遗传型克雅病患者的认识。方法 收集临床收治的一例以视觉症状为主的克雅病患者临床资料，并检索相关的文献，对其进行归纳总结并讨论。结果 患者女性，65岁，因视物颜色改变，视物变形就诊，入院后给予患者乙酰谷酰胺营养神经治疗，后完善相关的辅助检查后，确诊为一例遗传型克雅病患者，确诊后出院2个月时，患者死亡。结论 以视物变形，视物颜色改变的遗传型克雅病患者临床上并不常见，容易误诊、漏诊，通过本例病例可以提高临床医生对于此病的认识。
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