Dementia and geriatric cognitive disorders · 2013
Report about four novel mutations in the prion protein gene.
Клинический случайСтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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Schelzke Gabi, Stoeck Katharina, Eigenbrod Sabina, Grasbon-Frodl Eva, Raddatz Lena M, Ponto Claudia, Kretzschmar Hans A, Zerr Inga
Аннотация
BACKGROUND/AIMS: Since detection of the prion protein gene (PRNP) more than 30 mutations have been discovered. Some have only been found in single case reports without known intrafamilial accumulation or neuropathological proof so that the causal connection between mutation and disease could not be proved. Those patients often present atypical clinical phenotypes, and it is not unusual that they are classified as diseases other than Creutzfeldt-Jakob disease (CJD).
METHODS: Cases of suspected CJD have been reported to the national reference center for prion diseases. Clinical and diagnostic data were collected, and a classification of definite, possible or probable prion disease was made. Molecular analysis of PRNP was performed by capillary sequencing.
RESULTS: We have described 4 cases with atypical clinical and diagnostic findings and unknown mutations in PRNP so far.
CONCLUSION: Three patients fulfilled the criteria of probable CJD, and 1 patient fulfilled the criteria of possible CJD but the clinical picture in none of the patients was typical CJD; hence, it remained questionable whether the mutations were causal of the disease.
METHODS: Cases of suspected CJD have been reported to the national reference center for prion diseases. Clinical and diagnostic data were collected, and a classification of definite, possible or probable prion disease was made. Molecular analysis of PRNP was performed by capillary sequencing.
RESULTS: We have described 4 cases with atypical clinical and diagnostic findings and unknown mutations in PRNP so far.
CONCLUSION: Three patients fulfilled the criteria of probable CJD, and 1 patient fulfilled the criteria of possible CJD but the clinical picture in none of the patients was typical CJD; hence, it remained questionable whether the mutations were causal of the disease.