| Literature DB >> 18716560 |
Thomas E F Webb1, Suvankar Pal, Durrenajaf Siddique, Dominic C Heaney, Jacqueline M Linehan, Jonathan D F Wadsworth, Susan Joiner, Jon Beck, Stephen J Wroe, Valerie Stevenson, Sebastian Brandner, Simon Mead, John Collinge.
Abstract
Sibling concurrence of pathologically confirmed prion disease has only been reported in association with pathogenic mutation of the prion protein gene (PRNP). Here, we report 2 siblings with classic neuropathologic features of sporadic Creutzfeldt-Jakob disease unexplained by PRNP mutation or known risk factors for iatrogenic transmission of prion infection. Possible explanations include coincidental occurrence, common exposure to an unidentified environmental source of prions, horizontal transmission of disease, or the presence of unknown shared genetic predisposition.Entities:
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Year: 2008 PMID: 18716560 DOI: 10.1097/NEN.0b013e318182f36e
Source DB: PubMed Journal: J Neuropathol Exp Neurol ISSN: 0022-3069 Impact factor: 3.685