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Fatal Familial Insomnia : The Inheritance of Sleeplessness
Fatal Familial Insomnia is a rare, fatal, autosomal dominant neurodegenerative prion disease. FFI is caused by mutation in PRNP gene, causing misfolded proteins (prions) in the brain, particularly in thalamus, where sleep-wake cycle is controlled.
Yoon Shwe Yi Han
Mar 263 min read


Understanding Creutzfeldt-Jakob disease, CJD : A Closer Look at a Rare Brain Disorder
Creutzfeldt-Jakob Disease (CJD) is a rare, fatal brain disorder caused by misfolded prion proteins. These prions destroy brain cells, causing rapid dementia, coordination issues, and muscle spasms. With no cure, care focuses on symptom relief and comfort for patients and their families.
Yoon Shwe Yi Han
Dec 26, 20253 min read
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