familial Creutzfeldt-Jakob disease

出典: meddic


CJDCreutzfeldt-Jakob disease、Creutzfeldt-Jakob syndrome、new variant Creutzfeldt-Jakob diseasesubacute spongiform encephalopathy

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  • Creutzfeldt-Jakob disease and blood transfusion: updated results of the UK Transfusion Medicine Epidemiology Review Study.
  • Urwin PJ1, Mackenzie JM1, Llewelyn CA2, Will RG1, Hewitt PE3.
  • Vox sanguinis.Vox Sang.2015 Dec 28. doi: 10.1111/vox.12371. [Epub ahead of print]
  • BACKGROUND AND OBJECTIVES: This paper reports the results to 31 May 2015 of an ongoing UK study to look for additional cases of variant Creutzfeldt-Jakob disease (vCJD) transmission by blood transfusion, and to seek evidence whether other subtypes of Creutzfeldt-Jakob disease (CJD) may be transmissi
  • PMID 26709606
  • Prion Diseases.
  • Geschwind MD.
  • Continuum (Minneapolis, Minn.).Continuum (Minneap Minn).2015 Dec;21(6 Neuroinfectious Disease):1612-38. doi: 10.1212/CON.0000000000000251.
  • PURPOSE OF REVIEW: This article presents an update on the clinical aspects of human prion disease, including the wide spectrum of their presentations.RECENT FINDINGS: Prion diseases, a group of disorders caused by abnormally shaped proteins called prions, occur in sporadic (Jakob-Creutzfeldt disease
  • PMID 26633779
  • Early-onset spastic paraparesis as presenting sign of familial Creutzfeldt-Jakob disease.
  • Conte F1, Giordano A2, Tortora F3, Caiazzo G4, Ladogana A5, Tedeschi G6, Tessitore A7.
  • Parkinsonism & related disorders.Parkinsonism Relat Disord.2015 Dec;21(12):1479-80. doi: 10.1016/j.parkreldis.2015.10.004. Epub 2015 Oct 22.
  • PMID 26578040


  • プリオン病 : 本邦の特徴と診断のポイント
  • 三條 伸夫,水澤 英洋
  • 臨床神経学 50(5), 287-300, 2010-05-01
  • NAID 10026900121
  • Familial Creutzfeldt-Jakob disease with a V180I mutation: comparative analysis with pathological findings and diffusion-weighted images.
  • Mutsukura Kazuo,Satoh Katsuya,Shirabe Susumu,Tomita Itsuro,Fukutome Takayasu,Morikawa Minoru,Iseki Masachika,Sasaki Kensuke,Shiaga Yusei,Kitamoto Tetsuyuki,Eguchi Katsumi
  • Dementia and geriatric cognitive disorders 28(6), 550-557, 2009-12
  • … BACKGROUND: Diffusion-weighted imaging (DWI) has been reported to be a useful technique for diagnosing Creutzfeldt-Jakob disease (CJD). … The present study reported DWI results in cases of familial CJD with a V180I mutation (CJD180) in the prion protein gene as well as neurological findings. …
  • NAID 120002219591


The spectrum of neuropsychological features of familial Creutzfeldt-Jakob disease (CJD) have seldom been reported, possibly because of (a) the rarity of this he ... On the day of JD's admission, the neurology team requested a ...
1. Dement Geriatr Cogn Disord. 2009;28(6):550-7. doi: 10.1159/000254842. Epub 2009 Dec 30. Familial Creutzfeldt-Jakob disease with a V180I mutation: comparative analysis with pathological findings and diffusion ...


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先読みCJD」「Creutzfeldt-Jakob disease
リンク元家族性クロイツフェルト・ヤコブ病」「new variant Creutzfeldt-Jakob disease」「subacute spongiform encephalopathy


  [★] クロイツフェルト・ヤコブ病 Creutzfelt-Jakob病 Creutzfeldt-Jakob disease

Creutzfeldt-Jakob disease」

  [★] クロイツフェルト・ヤコブ病 CJD



familial Creutzfeldt-Jakob disease

new variant Creutzfeldt-Jakob disease」



CJDCreutzfeldt-Jakob disease、Creutzfeldt-Jakob syndrome、familial Creutzfeldt-Jakob diseasesubacute spongiform encephalopathy

subacute spongiform encephalopathy」



CJDCreutzfeldt-Jakob disease、Creutzfeldt-Jakob syndrome、familial Creutzfeldt-Jakob diseasenew variant Creutzfeldt-Jakob disease



  • n.
疾患illnessより厳密な概念。「ある臓器に明確な障害が確認され、それによって症状が出ているとはっきり説明できる場合」 (PSY.9)
特定の原因、病態生理、症状、経過、予後、病理組織所見が全てそろった場合 (PSY.9)
  • something that is very wrong with people's attitudes, way of life or with society.
ailailmentdisease entitydisorderillillnessmaladysicksickness
  • 注意

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「an impairment of health or a condition of abnormal functioning」

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「(体の)『病気』,疾患 / (精神・道徳などの)病気,病弊」

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「女性の話術芸人 =diseur」



  • adj.
  • 家族性の、家系性の、家族の
familyfamily memberhouseholdkindred

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「relating to or having the characteristics of a family; "children of the same familial background"; "familial aggregation"」

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「家族の,家族特有の / 違伝的な,血統にあらわれる」

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「occurring among members of a family usually by heredity; "an inherited disease"; "familial traits"; "genetically transmitted features"」
genetic, hereditary, inherited, transmitted, transmissible



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「caused by or altered by or manifesting disease or pathology; "diseased tonsils"; "a morbid growth"; "pathologic tissue"; "pathological bodily processes"」
morbid, pathologic, pathological

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「病気にかかった / 病的な,不健全な(morbid)」