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额颞叶痴呆

Frontotemporal dementia.

作者信息

Graff-Radford Neill R, Woodruff Bryan K

机构信息

Department of Neurology, Mayo College of Medicine, Mayo Clinic Jacksonville, Jacksonville, Florida 32224, USA.

出版信息

Semin Neurol. 2007 Feb;27(1):48-57. doi: 10.1055/s-2006-956755.

Abstract

Frontotemporal dementia (FTD) is an uncommon but important form of degenerative disease. It may make up 50% of dementia cases presenting before age 60. The symptoms are related to the anatomic areas affected. Neary divided the clinical syndromes into "frontotemporal dementia," "progressive nonfluent aphasia," and "semantic dementia." However, the pathology may extend beyond the frontal and temporal lobes and additional symptoms may be found. Although most cases are sporadic, some cases are genetic. The best-known genetic mutation causing FTD is frontotemporal dementia with parkinsonism, linked to the microtubule-associated protein tau on chromosome 17. There are other known genes and chromosome loci related to FTD. The most common pathology found is frontotemporal degeneration with ubiquitin inclusions. In contrast, FTD with Pick bodies is rare. Although there are strategies to help patients and their families, there is no known treatment for the disease.

摘要

额颞叶痴呆(FTD)是一种罕见但重要的退行性疾病。它可能占60岁前出现的痴呆病例的50%。症状与受影响的解剖区域有关。尼尔将临床综合征分为“额颞叶痴呆”、“进行性非流利性失语”和“语义性痴呆”。然而,病理改变可能超出额叶和颞叶,还可能发现其他症状。虽然大多数病例是散发性的,但有些病例是遗传性的。导致FTD最著名的基因突变是伴有帕金森综合征的额颞叶痴呆,与17号染色体上的微管相关蛋白tau有关。还有其他已知的与FTD相关的基因和染色体位点。最常见的病理表现是伴有泛素包涵体的额颞叶变性。相比之下,有Pick小体的FTD很少见。虽然有一些策略可以帮助患者及其家人,但目前尚无针对该疾病的已知治疗方法。

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