Literature DB >> 15364419

A novel presenilin 1 mutation (Y154N) in a patient with early onset Alzheimer's disease with spastic paraparesis.

Sayoko Hattori1, Kenji Sakuma, Yosuke Wakutani, Kenji Wada, Masaru Shimoda, Katsuya Urakami, Hisanori Kowa, Kenji Nakashima.   

Abstract

Early onset familial Alzheimer's disease with spastic paraparesis (FAD-SP) has been associated with mutations of the presenilin 1 gene (PSEN1). We report a pedigree of FAD-SP due to a novel missense mutation of PSEN1 (Y154N). The symptoms of the proband were characterized by presenile dementia in her 40s, preceded by spastic paraparesis in her 30s, whereas the mother of the proband presented with spastic paraparesis in her 40s, followed by symptoms of dementia in her mid 60s. The mutation was found only in the proband, and not in a normal family member, normal Japanese control subjects, patients with sporadic Alzheimer's disease or patients with familial spastic paraparesis without dementia. Thus, Y154N is a novel PSEN1 mutation responsible for FAD-SP of Japanese origin.

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Year:  2004        PMID: 15364419     DOI: 10.1016/j.neulet.2004.07.057

Source DB:  PubMed          Journal:  Neurosci Lett        ISSN: 0304-3940            Impact factor:   3.046


  9 in total

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Review 4.  Clinical phenotypic heterogeneity of Alzheimer's disease associated with mutations of the presenilin-1 gene.

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Review 5.  Mutations, associated with early-onset Alzheimer's disease, discovered in Asian countries.

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7.  Identification and Clinical Analysis of the First Nonsense Mutation in the PSEN1 Gene in a Family With Acute Encephalopathy and Retinitis Pigmentosa.

Authors:  Chunlin You; Weike Zeng; Lingna Deng; Zhihao Lei; Xinyi Gao; Victor Wei Zhang; Yidong Wang
Journal:  Front Neurol       Date:  2020-05-05       Impact factor: 4.003

8.  APP, PSEN1, and PSEN2 Mutations in Asian Patients with Early-Onset Alzheimer Disease.

Authors:  Vo Van Giau; Eva Bagyinszky; Young Chul Youn; Seong Soo A An; SangYun Kim
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  9 in total

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