Creutzfeldt-Jakob disease natural history, complications and prognosis: Difference between revisions

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{{‪Creutzfeldt-Jakob disease‬}}
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==Overview==
==Natural History==
==Complications==
==Complications==
* [[Infection]]
* [[Infection]]
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{{WikiDoc Sources}}
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[[Category:Infectious disease]]
[[Category:Infectious disease]]

Revision as of 20:41, 4 December 2012

Creutzfeldt-Jakob disease Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Creutzfeldt-Jakob disease from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

Diagnostic Study of Choice

History and Symptoms

Physical Examination

Laboratory Findings

Electrocardiogram

X-ray

Echocardiography and Ultrasound

CT scan

MRI

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Interventions

Surgery

Primary Prevention

Secondary Prevention

Cost-Effectiveness of Therapy

Future or Investigational Therapies

Case Studies

Case #1

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Complications

Prognosis

  • The outcome is usually very poor. Within 6 months or less of the onset of symptoms, the person will become incapable of self-care.
  • The disorder is fatal in a short time, usually within 8 months, but a few people survive as long as 1 or 2 years after diagnosis.

References


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