Article
Familial Creutzfeldt-Jakob Disease: Case report and role of genetic counseling in post mortem testing.
Prion - 1 Nov 2016
Clift Kristin, Guthrie Kimberly, Klee Eric W, Boczek Nicole, Cousin Margot, Blackburn Patrick, Atwal Paldeep
Abstract excerpt
Here we present a case of an asymptomatic 53-year-old woman who sought genetic testing for Familial Creutzfeldt-Jakob Disease (fCJD) after learning that her mother had fCJD. The patient's mother had a sudden onset of memory problems and rapidly deteriorating mental faculties in her late 70s, which led to difficulties ambulating, progressive non-fluent aphasia, dysphagia and death within ∼1 y of symptom onset. The...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
