Differentiating Oneiric Stupor in Agrypnia Excitata From Dreaming Disorders

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Agrypnia excitata and obstructive apnea in a patient with fatal familial insomnia from China

RATIONALE Fatal familial insomnia (FFI) linked to a D178N/129M haplotype mutation in the PRNP gene is the most common genetic prion disease in the Han Chinese population. Here, we describe a Han Chinese patient with FFI who exhibited agrypnia excitata and obstructive apnea. PATIENT CONCERNS A 46-year-old man displayed involuntary movements during sleep time, snoring, autonomic nervous system ...

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Dreaming and Eating Disorders

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ژورنال

عنوان ژورنال: Frontiers in Neurology

سال: 2020

ISSN: 1664-2295

DOI: 10.3389/fneur.2020.565694