成人发病性脑病因素缺乏症-一个病例报告
Dipti Baskar1, Vathsala Lakshmi1, Atchayaram Nalini1
1Department of Neurology, National Institute of Mental Health and Neuro Sciences (NIMHANS), Bengaluru, Karnataka, India.
Annals of Indian Academy of Neurology
|November 16, 2023
概括
患有情节性脑病变的成年人可能有素缺乏症 (CTLN2),这是一个罕见的疾病. 这个案例突出了新的症状,如肠道阻塞和脑部MRI在素缺乏的发现.
科学领域:
- 代谢障碍 代谢障碍 代谢障碍
- 神经科学是一个神经科学.
- 遗传学 是一个遗传学.
背景情况:
- 乙型素血症 (CTLN2) 是一种遗传性代谢障碍.
- 在成年人中,它可能会导致偶发性脑病变和妄.
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