Toward an early clinical diagnosis of MM2-type sporadic Creutzfeldt-Jakob disease.
Zhongyun ChenYu KongJing ZhangMin ChuLi LiuKexin XieYue CuiHong YeJunjie LiLin WangLiyong WuPublished in: Annals of clinical and translational neurology (2023)
In the absence of multiple typical sCJD symptoms within 6 months, the presence of cortical hyperintensity on DWI should raise concerns for MM2C-type sCJD after excluding other etiologies. Bilateral thalamic hypometabolism/hypoperfusion may be more helpful in the clinical diagnosis of MM2T-type sCJD.