格斯特曼 - 斯特劳斯勒 - 施林克病:一个病例报告
Journal of the Korean Society of Radiology
|June 16, 2023
概括
格斯特曼 - 斯特劳斯勒 - 施金克病是一种罕见的遗传性子疾病,表现为动力衰退和认知衰退. 基因检测证实了39岁男性的GSS疾病,具有特征性的MRI发现和家族病史.
科学领域:
- 神经科学是一个神经科学.
- 遗传学 是一个遗传学.
- 神经病理学神经病理学
背景情况:
- 格斯特曼 - 斯特劳斯勒 - 施克病 (GSS) 是一种罕见的,自体主导的,遗传性普里翁病.
- 它的特点是渐进的小脑缩,认知障碍和其他神经系统缺陷.
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