オスラー・ウェーバー・ランデュ病
WordNet
- an impairment of health or a condition of abnormal functioning
- German conductor and composer of romantic operas (1786-1826) (同)Carl Maria von Weber, Baron Karl Maria Friedrich Ernst von Weber
- German physiologist who studied sensory responses to stimuli and is considered the father of psychophysics (1795-1878) (同)E. H. Weber, Ernst Heinrich Weber
- German sociologist and pioneer of the analytic method in sociology (1864-1920) (同)Max Weber
- United States abstract painter (born in Russia) (1881-1961) (同)Max Weber
- German physicist and brother of E. H. Weber; noted for his studies of terrestrial magnetism (1804-1891) (同)Wilhelm Eduard Weber
- caused by or altered by or manifesting disease or pathology; "diseased tonsils"; "a morbid growth"; "pathologic tissue"; "pathological bodily processes" (同)morbid, pathologic, pathological
- a unit of magnetic flux equal to 100,000,000 maxwells (同)Wb
PrepTutorEJDIC
- (体の)『病気』,疾患 / (精神・道徳などの)病気,病弊
- 女性の話術芸人 =diseur
- 病気にかかった / 病的な,不健全な(morbid)
UpToDate Contents
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English Journal
- Living with hereditary haemorrhagic telangiectasia: Coping and psychological distress - A cross-sectional study.
- Geirdal AØ, Dheyauldeen S, Bachmann-Harildstad G, Heimdal K.SourceFaculty of Social Sciences, Oslo and Akershus University College of Applied Sciences , Oslo , Norway.
- Disability and rehabilitation.Disabil Rehabil.2013 Mar;35(5):206-13. doi: 10.3109/09638288.2012.690500. Epub 2012 Jun 7.
- Purpose: The purpose of this study was to examine the relationship between coping strategies measured by Coping Orientation to Problems Experienced Scale (COPE) and psychological distress measured by Hospital Anxiety and Depression Scale (HADS) and Becks Hopelessness Scale (BHS) in individuals livin
- PMID 22671535
- Argon plasma coagulation is an effective treatment for hereditary hemorrhagic telangiectasia patients with severe nosebleeds.
- Pagella F, Matti E, Chu F, Pusateri A, Tinelli C, Olivieri C, Canzonieri C, Boeri L, Ornati F, Danesino C.SourceDepartment of Otorhinolaryngology, University of Pavia and Foundation IRCCS Policlinico San Matteo.
- Acta oto-laryngologica.Acta Otolaryngol.2013 Feb;133(2):174-80. doi: 10.3109/00016489.2012.718097. Epub 2012 Oct 15.
- Abstract Conclusions: In contrast to the current trend according to which the treatment of hereditary hemorrhagic telangiectasia (HHT) epistaxis depends on clinical severity, argon plasma coagulation (APC) has also proven to be effective as a first-line procedure in patients with severe nosebleed
- PMID 23066781
- Reduced Mural Cell Coverage and Impaired Vessel Integrity After Angiogenic Stimulation in the Alk1-deficient Brain.
- Chen W, Guo Y, Walker EJ, Shen F, Jun K, Oh SP, Degos V, Lawton MT, Tihan T, Davalos D, Akassoglou K, Nelson J, Pile-Spellman J, Su H, Young WL.SourceDepartment of Anesthesia and Perioperative Care, University of California, San Francisco, 1001 Potrero Ave, Box 1363, San Francisco, CA 94110. hua.su@ucsf.edu.
- Arteriosclerosis, thrombosis, and vascular biology.Arterioscler Thromb Vasc Biol.2013 Feb;33(2):305-10. doi: 10.1161/ATVBAHA.112.300485. Epub 2012 Dec 13.
- OBJECTIVE: Vessels in brain arteriovenous malformations are prone to rupture. The underlying pathogenesis is not clear. Hereditary hemorrhagic telangiectasia type 2 patients with activin receptor-like kinase 1 (Alk1) mutation have a higher incidence of brain arteriovenous malformation than the gener
- PMID 23241407
Japanese Journal
- ITPと Osler-Rendu-Weber 病を併発した乳癌の1例
- 下代 玲奈,玄 東吉,岡本 浩之,宇田川 勝,谷畑 英一,稲留 征典
- 日本臨床外科学会雑誌 = The journal of the Japan Surgical Association 72(6), 1400-1404, 2011-06-25
- NAID 10029612273
- 遺伝性出血性血管拡張症(Osler 病)を合併した脛骨腓骨動脈瘤の1例
Related Links
- Osler-Weber-Rendu syndrome, or hereditary hemorrhagic telangiectasia (HHT), is a rare genetically determined disorder that affects blood vessels throughout the body and results in a tendency for bleeding. HHT is an autosomal dominant disorder characterized by vascular dysplasia and hemorrhage.
- 遺伝性出血性毛細血管拡張症 Hereditary hemorrhagic telangiectasia (HHT) Osler-Weber-Rendu disease 遺伝性出血性毛細血管拡張症 (HHTと略します)は、全身の血管に異常が起こり、出血傾向の出る常染色体優性の遺伝性疾患 ...
★リンクテーブル★
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- 英
- Osler-Weber-Rendu disease
- 同
- Osler-Weber-Rendu病、遺伝性出血性毛細血管拡張 hereditary hemorrhagic telangiectasia
- オスラー・ウェーバー・ランデュ症候群 Osler-Weber-Rendu syndrome(HIM)
- 関
- 肺動静脈瘻
[show details]
ja
Osler-Rendu-Weber disease : 50 件
Osler-Weber-Rendu disease : 約 915 件
Rendu-Osler-Weber disease : 約 86 件
Rendu-Weber-Osler disease : nothing
Weber-Osler-Rendu disease : 4 件
Weber-Rendu-Osler disease : 4 件
Osler-Rendu-Weber syndrome : 約 49 件
Osler-Weber-Rendu syndrome : 83 件
Rendu-Osler-Weber syndrome : 80 件
Rendu-Weber-Osler syndrome : 1 件
Weber-Osler-Rendu syndrome : 4 件
Weber-Rendu-Osler syndrome : nothing
en
Osler-Rendu-Weber disease : 約 5,830 件
Osler-Weber-Rendu disease : 約 22,100 件
Rendu-Osler-Weber disease : 約 23,500 件
Rendu-Weber-Osler disease : 約 78 件
Weber-Osler-Rendu disease : 27 件
Weber-Rendu-Osler disease : 約 79 件
Osler-Rendu-Weber syndrome : 約 7,610 件
Osler-Weber-Rendu syndrome : 約 41,500 件
Rendu-Osler-Weber syndrome : 約 8,890 件
Rendu-Weber-Osler syndrome : 約 34 件
Weber-Osler-Rendu syndrome : 約 46 件
Weber-Rendu-Osler syndrome : 7 件
オスラー・ランデュ・ウェーバー病 : 9 件
オスラー・ウェーバー・ランデュ病 : 32 件
ランデュ・オスラー・ウェーバー病 : 10 件
ランデュ・ウェーバー・オスラー病 : nothing
ウェーバー・オスラー・ランデュ病 : 4 件
ウェーバー・ランデュ・オスラー病 : nothing
オスラー・ランデュ・ウェーバー症候群 : 4 件
オスラー・ウェーバー・ランデュ症候群 : 9 件
ランデュ・オスラー・ウェーバー症候群 : 29 件
ランデュ・ウェーバー・オスラー症候群 : nothing
ウェーバー・オスラー・ランデュ症候群 : 2 件
ウェーバー・ランデュ・オスラー症候群 : nothing
- 常染色体優性遺伝
- 全身の毛細血管拡張により、チアノーゼ、手足のばち指、赤血球増多症、各種出血症状(喀血、脳・胃・腸管出血)をきたす (SSUR.330)
- 症例の15%に肺動静脈瘻を合併する(YN.I-120)
参考
- 1. TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER; HHTAl - OMIM
- OSLER-RENDU-WEBER DISEASE
- ORW DISEASE
- Gene map locus: 9q34.1
- http://omim.org/entry/187300
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- 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.
- 関
- ail、ailment、disease entity、disorder、ill、illness、malady、sick、sickness
- disease ≠ illness ≠ disorder
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ウェーバー