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CJD (medical condition): Creutzfeldt-Jakob Disease (CJD) is a rare 1-in-a-million disease that occurs spontaneously, with 10-15% inheritance, and unrelated ...more
CJD: See also:
Creutzfeldt-Jakob Disease:
»Introduction: Creutzfeldt-Jakob Disease
»Symptoms of Creutzfeldt-Jakob Disease
»Treatments for Creutzfeldt-Jakob Disease
CJD: Abbreviation for Creutzfeldt-Jakob disease.
Source: Stedman's Medical Spellchecker, © 2006 Lippincott Williams & Wilkins. All rights reserved.
CJD: A rare transmissible encephalopathy most prevalent between the ages of 50 and 70 years. Affected individuals may present with sleep disturbances, personality changes, ATAXIA; APHASIA, visual loss, weakness, muscle atrophy, MYOCLONUS, progressive dementia, and death within one year of disease onset. A familial form exhibiting autosomal dominant inheritance and a new variant CJD (potentially associated with ENCEPHALOPATHY, BOVINE SPONGIFORM) have been described. Pathological features include prominent cerebellar and cerebral cortical spongiform degeneration and the presence of PRIONS. (From N Engl J Med, 1998 Dec 31;339(27))
Source: Diseases Database
These medical condition or symptom topics may be relevant to medical information for CJD:
CJD is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that CJD, or a subtype of CJD,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
CJD: Another name for Creutzfeldt-Jakob Disease (or close medical condition association).
»Introduction: Creutzfeldt-Jakob Disease
»Symptoms of Creutzfeldt-Jakob Disease
»Treatments for Creutzfeldt-Jakob Disease
CJD: CJD is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of CJD incude:
See full list of 37 symptoms of CJD (Creutzfeldt-Jakob Disease)
Treatments for CJD (Creutzfeldt-Jakob Disease) include:
Read more about treatments for CJD
Treatment of CJD: For more treatment information about CJD, see treatment of Creutzfeldt-Jakob Disease (CJD)
Creutzfeldt-Jakob disease (CJD) is a rare, degenerative, invariably fatal brain disorder. It... (Source: excerpt from Creutzfeldt-Jakob Disease Fact Sheet: NINDS)
Creutzfeldt-Jakob disease (CJD) is a rare, degenerative, invariably fatal brain disorder. Typically, onset of symptoms... (Source: excerpt from NINDS Creutzfeldt-Jakob Disease Information Page: NINDS)
Creutzfeldt-Jakob disease (CJD) is a rare, degenerative, invariably fatal brain disorder. It affects about... (Source: excerpt from Creutzfeldt-Jakob Disease Fact Sheet: NINDS)
Creutzfeldt-Jakob Disease (CJD) is a progressive neurological disorder which belongs to a group of degenerative... (Source: excerpt from Facts About Creutzfeldt-Jakob Disease: CDC-OC)
These medical disease topics may be related to CJD:
Source: Diseases Database
Source - NIH
Source: Diseases Database
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