TY  - GEN
N2  - The most common prion disease is Creutzfeldt-Jacob disease (CJD), usually sporadic (sCJD), but in up to 15% familial due to mutations in the prion gene. CJD presents with myoclonis, ataxia, and rapidly progressive dementia with an average age of onset of 67 years. Fatal Familial Insomnia (FFI) is a related uniformly fatal prion disease, with mean onset of dysautonomia and insomnia at 56 years and mean duration of 13 months.
DO  - 10.6083/gb19f633j
DO  - DOI
AB  - The most common prion disease is Creutzfeldt-Jacob disease (CJD), usually sporadic (sCJD), but in up to 15% familial due to mutations in the prion gene. CJD presents with myoclonis, ataxia, and rapidly progressive dementia with an average age of onset of 67 years. Fatal Familial Insomnia (FFI) is a related uniformly fatal prion disease, with mean onset of dysautonomia and insomnia at 56 years and mean duration of 13 months.
AD  - Oregon Health and Science University
AD  - Oregon Health and Science University
T1  - Sporadic fatal insomnia: a case report
DA  - 2020
AU  - Alrohaibani, Alaaeddin
AU  - Woltjer, Randall
L1  - https://digitalcollections.ohsu.edu/record/8346/files/ResearchWeek.2020.Alrohaibani.Alaaeddin.pdf
PB  - Oregon Health and Science University
LA  - eng
PY  - 2020
ID  - 8346
L4  - https://digitalcollections.ohsu.edu/record/8346/files/ResearchWeek.2020.Alrohaibani.Alaaeddin.pdf
KW  - Creutzfeldt-Jakob Syndrome
KW  - Insomnia, Fatal Familial
KW  - Prion Diseases
KW  - Neurodegenerative Diseases
KW  - fatal familial insomnia
KW  - sporadic fatal insomnia
KW  - sleep disorders
TI  - Sporadic fatal insomnia: a case report
Y1  - 2020
L2  - https://digitalcollections.ohsu.edu/record/8346/files/ResearchWeek.2020.Alrohaibani.Alaaeddin.pdf
LK  - https://digitalcollections.ohsu.edu/record/8346/files/ResearchWeek.2020.Alrohaibani.Alaaeddin.pdf
UR  - https://digitalcollections.ohsu.edu/record/8346/files/ResearchWeek.2020.Alrohaibani.Alaaeddin.pdf
ER  -