Search results
Results from the WOW.Com Content Network
Fatal insomnia is an extremely rare neurodegenerative prion disease that results in trouble sleeping as its hallmark symptom. [2] The majority of cases are familial ( fatal familial insomnia [FFI]), stemming from a mutation in the PRNP gene, with the remainder of cases occurring sporadically ( sporadic fatal insomnia [sFI]).
Fatal insomnia is a neurodegenerative disease that eventually results in a complete inability to go past stage 1 of NREM sleep. In addition to insomnia, patients may experience panic attacks, paranoia, phobias, hallucinations, rapid weight loss, and dementia. Death usually occurs between 7 and 36 months from onset. [citation needed]
Cases of objective total insomnia are extremely rare. The few that have been recorded have predominantly been ascribed to a rare incurable genetic disorder called fatal familial insomnia, which patients rarely survive for more than 26 months after the onset of illness—often much less. [19]
Insomnia is one of the most common sleep disorders, with the Centers for Disease Control and Prevention reporting that as many as one in two adults experience short-term bouts, while one in 10 may ...
For premium support please call: 800-290-4726 more ways to reach us
Fatal familial insomnia, an extremely rare and universally-fatal prion disease that causes a complete cessation of sleep. Hypopnea syndrome, abnormally shallow breathing or slow respiratory rate while sleeping. Idiopathic hypersomnia, a primary, neurologic cause of long-sleeping, sharing many similarities with narcolepsy. [83]
Rare Transmissible spongiform encephalopathies ( TSEs ), also known as prion diseases , [ 1 ] are a group of progressive, incurable, and fatal conditions that are associated with the prion hypothesis and affect the brain and nervous system of many animals , including humans , cattle , and sheep .
For premium support please call: 800-290-4726 more ways to reach us