Literature DB >> 17943067

Fatal familial insomnia and agrypnia excitata.

Elio Lugaresi1, Federica Provini.   

Abstract

This review summarizes the pioneering steps culminating in the identification of a novel disease, fatal familial insomnia (FFI), a hereditary prion disease. Together with Morvan's chorea and delirium tremens, FFI is characterized by an inability to sleep associated with motor and autonomic overactivation. We named this pattern agrypnia excitata, a syndrome caused by a dysfunction in thalamolimbic circuits. This review highlights the strategic role of the limbic thalamus in the central autonomic network running from the limbic cortex to the lower brainstem and regulating sleep and wakefulness.

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Year:  2007        PMID: 17943067

Source DB:  PubMed          Journal:  Rev Neurol Dis        ISSN: 1545-2913


  4 in total

Review 1.  Agrypnia excitata.

Authors:  Federica Provini
Journal:  Curr Neurol Neurosci Rep       Date:  2013-04       Impact factor: 5.081

Review 2.  The genetic and molecular regulation of sleep: from fruit flies to humans.

Authors:  Chiara Cirelli
Journal:  Nat Rev Neurosci       Date:  2009-08       Impact factor: 34.870

Review 3.  Genetic studies in human prion diseases.

Authors:  Byung-Hoon Jeong; Yong-Sun Kim
Journal:  J Korean Med Sci       Date:  2014-04-25       Impact factor: 2.153

Review 4.  Differentiating Oneiric Stupor in Agrypnia Excitata From Dreaming Disorders.

Authors:  Luca Baldelli; Federica Provini
Journal:  Front Neurol       Date:  2020-11-12       Impact factor: 4.003

  4 in total

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