Creutzfeldt-Jakob disease: A case report and differential diagnoses

被引：2

作者：

Raut, Akash ^{[1
]}

Thapa, Anjila ^{[1
]}

Shrestha, Ashish ^{[2
]}

Saud, Kamal ^{[2
]}

Rajbhandari, Reema ^{[2
]}

Katwal, Shailendra ^{[3
]}

机构：

[1] Inst Med, Maharajgunj Med Campus, Kathmandu, Nepal

[2] Tribhuvan Univ Teaching Hosp, Dept Neurol, Kathmandu, Nepal

[3] Tribhuvan Univ Teaching Hosp, Dept Radiol, Kathmandu, Nepal

来源：

CLINICAL CASE REPORTS | 2022年 / 10卷 / 08期

关键词：

neurodegeneration; psychoneuroimmunology; prion disease; sporadic Creutzfeldt-Jakob disease; CEREBROSPINAL-FLUID; PRION PROTEIN; SYMPTOMS; FEATURES;

D O I：

10.1002/ccr3.6239

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Although sporadic Creutzfeldt-Jakob disease is a rare neurodegenerative disease and often difficult to diagnose at the earliest onset, meticulous clinical examination, electroencephalography, and neuroimaging findings will help in diagnosis.

引用

页数：5

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