Creutzfeldt-Jakob Syndrome
                             
                            
                            
                                
                            
                            
                                
                            
                            
                            
                                
                                    
                                            
	"Creutzfeldt-Jakob Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, 
	MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, 
	which enables searching at various levels of specificity.
	
	
		
			
			
				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))
    
			
			
				
				
					
						| Descriptor ID | D007562 | 
					
						| MeSH Number(s) | C10.228.140.380.165 C10.228.228.800.230 F03.615.400.300 | 
					
						| Concept/Terms | Creutzfeldt-Jakob SyndromeCreutzfeldt-Jakob SyndromeCreutzfeldt Jakob SyndromeSyndrome, Creutzfeldt-JakobCreutzfeldt-Jakob DiseaseCreutzfeldt Jakob DiseaseDisease, Creutzfeldt-JakobJakob-Creutzfeldt DiseaseDisease, Jakob-CreutzfeldtJakob Creutzfeldt DiseaseCJD (Creutzfeldt-Jakob Disease)CJD (Creutzfeldt Jakob Disease)Spongiform Encephalopathy, SubacuteEncephalopathies, Subacute SpongiformEncephalopathy, Subacute SpongiformSpongiform Encephalopathies, SubacuteSubacute Spongiform EncephalopathiesSubacute Spongiform EncephalopathyCreutzfeldt Jacob DiseaseDisease, Creutzfeldt JacobJacob Disease, CreutzfeldtJakob-Creutzfeldt SyndromeJakob Creutzfeldt SyndromeSyndrome, Jakob-Creutzfeldt
 Creutzfeldt-Jakob Disease, FamilialCreutzfeldt-Jakob Disease, FamilialCreutzfeldt Jakob Disease, FamilialCreutzfeldt-Jakob Diseases, FamilialDisease, Familial Creutzfeldt-JakobFamilial Creutzfeldt-Jakob DiseasesFamilial Creutzfeldt-Jakob DiseaseFamilial Creutzfeldt Jakob Disease
 New Variant Creutzfeldt-Jakob DiseaseNew Variant Creutzfeldt-Jakob DiseaseNew Variant Creutzfeldt Jakob DiseaseCreutzfeldt-Jakob Disease, VariantCreutzfeldt Jakob Disease, VariantCreutzfeldt-Jakob Disease, New VariantCreutzfeldt Jakob Disease, New VariantVariant Creutzfeldt-Jakob DiseaseVariant Creutzfeldt Jakob DiseaseV-CJD (Variant-Creutzfeldt-Jakob Disease)V CJD (Variant Creutzfeldt Jakob Disease)
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				Below are MeSH descriptors whose meaning is more general than "Creutzfeldt-Jakob Syndrome".
				
			 
			
			
				Below are MeSH descriptors whose meaning is more specific than "Creutzfeldt-Jakob Syndrome".
				
			 
		 
	 
 
                                        
                                            
	
	
		
			
			
					
				This graph shows the total number of publications written about "Creutzfeldt-Jakob Syndrome" by people in this website by year, and whether "Creutzfeldt-Jakob Syndrome" was a major or minor topic of these publications. 
				
					 
                    To see the data from this visualization as text, 
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		            | Year | Major Topic | Minor Topic | Total | 
|---|
| 2003 | 1 | 0 | 1 | 
| 2013 | 0 | 1 | 1 | 
| 2017 | 1 | 0 | 1 | 
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				Below are the most recent publications written about "Creutzfeldt-Jakob Syndrome" by people in Profiles.
						
					
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								Rossi KC, Stahl CM, Zhang P, Liang JW, Marcuse LV, Lublin F. Sporadic Creutzfeldt-Jakob Disease With Unilateral Symptoms in the Setting of Metastatic Renal Cell Carcinoma. Neurologist. 2017 Jul; 22(4):131-133. 
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								Jackson WS, Borkowski AW, Watson NE, King OD, Faas H, Jasanoff A, Lindquist S. Profoundly different prion diseases in knock-in mice carrying single PrP codon substitutions associated with human diseases. Proc Natl Acad Sci U S A. 2013 Sep 03; 110(36):14759-64. 
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								Drachman DA. Comment: Tau vs 14-3-3 protein--adjuncts for the diagnosis of CJD. Neurology. 2012 Aug 07; 79(6):551. 
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								Tschampa HJ, M?rtz P, Flacke S, Paus S, Schild HH, Urbach H. Thalamic involvement in sporadic Creutzfeldt-Jakob disease: a diffusion-weighted MR imaging study. AJNR Am J Neuroradiol. 2003 May; 24(5):908-15. 
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								Morris AH, Reiter EO. Growth hormone: diagnostic and therapeutic dilemmas. Semin Adolesc Med. 1987 Dec; 3(4):283-91. 
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								Smith TW, Anwer U, DeGirolami U, Drachman DA. Vacuolar change in Alzheimer's disease. Arch Neurol. 1987 Dec; 44(12):1225-8.