MM1 variant of sporadic Creutzfeldt-Jakob disease with long duration akinetic mutism state;Enfermedad de Creutzfeldt-Jakob esporádica, variante MM1, asociada a mutismo acinético de larga duración

Neurologia

Volumn 21, Issue 8, 2006, Pages 444-446

  Sanchez Valle R ^a   Santamaria, J ^a   Rey, M J ^a   Rodriguez A ^a   Graus, F ^a   Saiz, Albert ^a,b  

^a UNIVERSITY OF BARCELONA   (Spain)

^b HOSPITAL CLÍNIC   (Spain)

Author keywords

14 3 3 assay; Akinetic mutism; Creutzfeldt Jakob syndrome; Magnetic resonance imaging; Prion disease

Indexed keywords

AKINETIC MUTISM; ARTICLE; CASE REPORT; CREUTZFELDT JAKOB DISEASE; FATALITY; FEMALE; HUMAN; MIDDLE AGED; PATHOLOGY; SURVIVAL RATE;

AKINETIC MUTISM; CREUTZFELDT-JAKOB SYNDROME; FATAL OUTCOME; FEMALE; HUMANS; MIDDLE AGED; SURVIVAL RATE;

EID: 39049184780     PISSN: 02134853     EISSN: 15781968     Source Type: Journal    
DOI: None     Document Type: Article

References (11)

1. Tschampa HJ, Kallenberg K, Urbach H, Meissner B, Nicolay C, Kretzschmar HA, et al. MRI in the diagnosis of sporadic Creutzfeldt-Jakob disease: a study on inter-observer agreement. Brain 2005;128:2026-33.
2. Zerr I, Schulz-Schaeffer WJ, Giese A, Bodemer M, Schröter A, Henkel K, et al. Current clinical diagnosis in Creutzfeldt-Jakob disease: identification of uncommon variants. Ann Neurol 2000;48:323-9.
3. Parchi P, Giese A, Capellari S, Brown P, Schulz-Schaeffer WJ, Windl O, et al. Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects. Ann Neurol 1999;46:224-33.
4. Sánchez-Valle R, Nos C, Yagüe J, Graus F, Domínguez A, Saiz A, for the Catalan Collaborative Study Group for CJD. Clinical and genetic features of human prion diseases in Catalonia. Eur J Neurol 2004;11:649-55.
5. Brown P, Rodgers-Johnson P, Cathala F, Gibbs C, Gajdusek DC. Creutzfeldt-Jakob disease of long duration: clinicopahological characteristics, transmissibility, and differential diagnosis. Ann Neurol 1984;16:295-304.
6. Pocchiari M, Puopolo M, Croes EA, Budka H, Gelpi E, Collins S, et al. Predictors of survival in sporadic Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies. Brain 2004;127:2348-59.
7. Otto A, Zerr I, Lantsch M, Weidehaas K, Riedemann C, Poser S. Akinetic mutism as a classification criterion for the diagnosis of Creutzfeldt-Jakob disease. J Neurol Neurosurg Psychiatry 1998;64:524-8.
8. Matsusue E, Kinoshita T, Sugihara S, Fujii S, Ogawa T, Ohama E. White matter lesions in panencephalopathic type of Creutzfeldt-Jakob disease: MR imaging and pathologic correlations. Am J Neuroradiol 2004;25:910-8.
9. Ghorayeb I, Series C, Parchi P, Sawan M, Guez S, Laplanche JL, et al. Creutzfeldt-Jakob disease with long duration and panencephalopathic lesions: molecular analysis of one case. Neurology 1998;51:271-4.
10. Meissner B, Westner IM, Kallenberg K, Krasnianski A, Bartl M, Varges D, et al. Sporadic Creutzfeldt-Jakob disease: clinical and diagnostic characteristics of the rare VV1 type. Neurology 2005;65:1544-50.
11. Binelli S, Agazzi P, Giaccone G, Will RG, Bugiani O, Franceschetti S, et al. Periodic electroencephalogram complexes in a patient with variant Creutzfeldt-Jakob disease. Ann Neurol 2006;59:423-7.