Agrypnia excitata and obstructive apnea in a patient with fatal familial insomnia from China: A case report

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-y...

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Detalles Bibliográficos
Autores principales: Sun, Congcong, Xia, Wen, Liu, Ying, Jia, Guoyong, Wang, Cuilan, Yan, Chuanzhu, Li, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2017
Materias:
5300
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5728880/
https://www.ncbi.nlm.nih.gov/pubmed/29245265
http://dx.doi.org/10.1097/MD.0000000000008951

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5728880/
https://www.ncbi.nlm.nih.gov/pubmed/29245265
http://dx.doi.org/10.1097/MD.0000000000008951

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