家族性前頭側頭型認知症
WordNet
- relating to or having the characteristics of a family; "children of the same familial background"; "familial aggregation"
- occurring among members of a family usually by heredity; "an inherited disease"; "familial traits"; "genetically transmitted features" (同)genetic, hereditary, inherited, transmitted, transmissible
- mental deterioration of organic or functional origin (同)dementedness
PrepTutorEJDIC
- 家族の,家族特有の / 違伝的な,血統にあらわれる
- (医学的な)痴呆(ちほう)
UpToDate Contents
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English Journal
Japanese Journal
- Progranulin haploinsufficiency reduces amyloid beta deposition in Alzheimer's disease model mice
- HOSOKAWA Masato,TANAKA Yoshinori,ARAI Tetsuaki,KONDO Hiromi,AKIYAMA Haruhiko,HASEGAWA Masato
- 実験動物彙報 67(1), 63-70, 2018
- … <p>Granulin (<i>Grn</i>) mutations were identified in familial frontotemporal lobar degeneration (FTLD) patients with TAR DNA-binding protein of 43 kd (TDP-43) pathology. …
- NAID 130006339997
- さまざまな認知症との出会い―Pick-like presenile dementia with ALS, Gerstmann-Sträussler-Scheinker 病, レビー小体病, パーキンソン・認知症複合など
- 葛原 茂樹
- 高次脳機能研究 （旧 失語症研究） 37(2), 187-194, 2017
- … 1970 年代に経験した Pick 病様の前頭側頭型認知症を伴う筋萎縮性側索硬化症 (ALS) 症例は, 現代の TDP proteinopathy の一型である frontotemporal dementia-ALS であった。 …
- NAID 130007387985
- 太田 康之,阿部 康二
- 神経治療学 34(2), 107-111, 2017
- … Recent reports showed sporadic and familial amyotrophic lateral sclerosis (ALS)/frontotemporal dementia (FTD) in the Caucasian population is caused by hexanucleotide GGGGCC repeat expansion in intron 1 of the C9orf72 gene, similar to the genetic mutation in Asidan patients. …
- NAID 130005858970
Related Links
- Frontotemporal dementia (FTD) is second only to Alzheimer’s disease as a cause of dementia. It is mainly sporadic but may be familial, often with a mutation (P301L) in the tau gene. Behavioural and language disturbances are ...
- 1. Neurology. 1998 Jun;50(6):1541-5. Familial aggregation in frontotemporal dementia. Stevens M, van Duijn CM, Kamphorst W, de Knijff P, Heutink P, van Gool WA, Scheltens P, Ravid R, Oostra BA, Niermeijer MF, van Swieten JC.
★リンクテーブル★
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- 英
- familial frontotemporal dementia
- 関
- 前頭側頭型認知症
- 第17 染色体遺伝子に連鎖しパーキンソニズムを伴う家族性前頭側頭型認知症(frontotemporal dementia and parkinsonism linked to chromosome 17)(FTDP-17)の病因はMAPT遺伝子の変異。
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- 関
- family、family member、household、kindred
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- 関
- dementia、dementing、deterioration