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Difficult case of a rare form of familial Alzheimer’s disease with PSEN1 P117L mutation
Less than 10% of Alzheimer’s disease (AD) cases are familial. Presenilin-1 (PSEN1) mutations are the most frequent aetiology and may be associated to atypical neurological manifestations. We report the case of a 27-year-old right-handed man, ensuing with mild cognitive impairment, motor discoordinat...
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| Yayımlandı: | BMJ Case Rep |
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| Asıl Yazarlar: | , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
BMJ Publishing Group
2018
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6301458/ https://ncbi.nlm.nih.gov/pubmed/30567237 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2018-226664 |
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