FFI: Fatal Family Insomnia
This is a news story, published by Live Science, that relates primarily to FFI news.
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neurodegenerative prion diseaseLive Science
•Health
Health
Fatal familial insomnia: a genetic condition where people never sleep again

77% Informative
FFI is a neurodegenerative prion disease that is caused by a mutation in a gene called PRNP .
Symptoms usually begin around 40 , but can develop as early as 20 or as late as 70.
Patients with FFI also commonly experience memory loss, high blood pressure, hallucinations and involuntary jerking of their muscles.
Patients typically die within nine to 30 months after symptoms emerge.
VR Score
81
Informative language
80
Neutral language
80
Article tone
informal
Language
English
Language complexity
52
Offensive language
not offensive
Hate speech
not hateful
Attention-grabbing headline
not detected
Known propaganda techniques
not detected
Time-value
long-living
External references
12
Source diversity
10