Creutzfeldt-Jacob disease is a rare and fatal prion disease comprised of four variants: familial, sporadic, variant, and iatrogenic. Classic presenting symptoms include a rapidly progressive dementia, myoclonus, and ataxia. Misdiagnosis often occurs due to the neuropsychiatric phenotypic variability of CJD. Psychiatric manifestations across all four types of CJD are now increasingly being recog...

Creutzfeldt-Jacob disease is a rare, neurodegenerative disease caused by a prion protein. The patients are usually between 40 and 60 years old. Most of the patients die within one year after onset of the disease. A typical case is reported. It is pointed out that such a dramatic development can cause anxiety and a feeling of inadequacy for close relatives. To avoid adverse consequences, it is i...

Submit Manuscript | http://medcraveonline.com benign bone tumors and %8-15 of all primary bone tumors. The World Health Organization describes the OC as a cartilage-capped bony protrusion on the external surface of bone [1]. Although Von Langenbeck defined coronoid process hyperplasia in 1853, Jacob first described OC of the coronoid process forming pseudojoint between the coronoid process and ...