Fatal familial insomnia with abnormal signals on routine MRI: a case report and literature review
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DOI: 10.1186/s12883-017-0886-2
Abstract: BackgroundFatal familial insomnia (FFI) is a rare autosomal dominant disease caused by the PRNP D178N/129 M mutation. Routine brain CT and MRI usually reveal non-specific features. We report a patient with FFI presenting with diffuse abnormal… read more here.
Keywords: abnormal signals; insomnia abnormal; case; familial insomnia ... See more keywords