Lautenschlager Nicola T, Martins Ralph N
University of Western Australia, School of Psychiatry and Clinical Neurosciences, Mail Delivery Point M573, 35 Stirling Highway, Crawley, Perth, WA 6009, Australia.
Int Psychogeriatr. 2005;17 Suppl 1:S27-34. doi: 10.1017/s1041610205002000.
When patients present with a dementia syndrome at a young age, the experienced clinician will automatically include uncommon dementias in the diagnostic considerations, as familial uncommon dementias due to genetic mutations frequently present as early-onset dementias. This paper highlights why uncommon dementias due to genetic mutations, although marginal in terms of prevalence numbers in the total population, are of significance in the quest to unravel the underlying cause of common dementias such as Alzheimer's disease (AD), dementia with Lewy bodies (DLB), frontotemporal dementias (FTD) and vascular dementia (VaD).
当患者在年轻时出现痴呆综合征时,经验丰富的临床医生会自动将罕见痴呆纳入诊断考虑范围,因为由基因突变引起的家族性罕见痴呆通常表现为早发性痴呆。本文强调了为什么尽管基因突变导致的罕见痴呆在总人口中的患病率较低,但在探寻常见痴呆(如阿尔茨海默病(AD)、路易体痴呆(DLB)、额颞叶痴呆(FTD)和血管性痴呆(VaD))的潜在病因方面具有重要意义。