Creutzfeldt-Jakob's Disease Within the Superficial Occipital Lobe (Subacute Spongiform Encephalopathy)

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Creutzfeldt-Jakob's Disease, also known as variant CJD
Is a prion-caused neurodegenerative disorder with diagnostic and clinical characteristic Features
It progresses more rapidly than any bacterial infection and has a 100% mortality rate

Bacterially!
Infestationally!

Invariably fatal
Cellular glycoprotein
Abnormal isoform
Prion mutation
Occurs worldwide

There are about 1.5 out of 1 million cases every year

Slow degeneration
Of mental operations

There is no known cure
100% death rate
Gradual increase in hallucinations
Aggressive behavior spikes

Onset of dementia, delayed neurological function
Pulvinar sign on MRI, present in most cases
Immunohistochemically analysis
Brain tissue disintegration

Lymphoid tissue agent presence
Increased levels of glycoform
Analysis of prion proteins
Protease-resistance

Readily detected, paranoia, psychosis
Draining of cerebrovascular fluids
Accident during cerebral resection
Mortification begins again

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