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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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| Publié dans: | Medicine (Baltimore) |
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| Auteurs principaux: | , , , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Wolters Kluwer Health
2017
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5728880/ https://ncbi.nlm.nih.gov/pubmed/29245265 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000008951 |
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