与偏偏甲状腺功能障碍相关的法尔综合征:一个病例报告
Mukesh Kumar Sarna1, Pallaavi Goel2, Varun Bhargava2
1Department of General Medicine, Mahatma Gandhi Medical College and Hospital, Jaipur, India.
The journal of the Royal College of Physicians of Edinburgh
|November 8, 2023
概括
法尔综合征是一种罕见的遗传神经系统疾病,涉及大脑沉积. 这一案例突出了它与缺甲状腺症的关联,有助于诊断和症状治疗.
科学领域:
- 神经学 神经学
- 遗传学 是一个遗传学.
- 放射学 放射学是一门学科.
背景情况:
- 法尔综合征是一种罕见的遗传神经疾病,其特点是大脑控制运动的区域中异常的沉积.
- 它影响的不到10万个人中的1个,通常是年轻到中年成年人.
- 症状包括额外的pyramidal标志,小脑功能障碍,语言障碍,痴呆症和神经精神问题.
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