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Dr. Shoyeb
এমবিবিএস
,
পিজিটি(মেডিসিন)
,
সিসিডি(বারডেম)
,
সিএমইউ
Fatal familial insomnia: Abbreviated FFI. An hereditary prion disease characterized by disrupted sleep ( insomnia), motor abnormalities (myoclonus, ataxia, dysarthria, dysphagia, and pyramidal signs), and hyperactivation of the autonomic nervous system. Due to a missense mutation at codon 178 of the prion protein gene on chromosome 20. A sporadic form of fatal insomnia is also known.
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