WordNet
- a pattern of symptoms indicative of some disease
- a complex of concurrent things; "every word has a syndrome of meanings"
PrepTutorEJDIC
- (疾患の徴候となる一群の)症徴候,症候群 / (事件・社会的状態などのパターンを示す)徴候形態
- まつげ(eyelashes) / 繊毛
UpToDate Contents
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English Journal
- Respiratory motile cilia dysfunction in a patient with cranioectodermal dysplasia.
- Li Y1, Garrod AS2, Madan-Khetarpal S3, Sreedher G3, McGuire M3,4, Yagi H1, Klena NT1, Gabriel GC1, Khalifa O, Zahid M1, Panigrahy A5, Weiner DJ2, Lo CW1.
- American journal of medical genetics. Part A.Am J Med Genet A.2015 Sep;167A(9):2188-96. doi: 10.1002/ajmg.a.37133. Epub 2015 Apr 25.
- Ciliopathies such as cranioectodermal dysplasia, Sensenbrenner syndrome, short-rib polydactyly, and Jeune syndrome are associated with respiratory complications arising from rib cage dysplasia. While such ciliopathies have been demonstrated to involve primary cilia defects, we show motile cilia dysf
- PMID 25914204
- CCDC65 mutation causes primary ciliary dyskinesia with normal ultrastructure and hyperkinetic cilia.
- Horani A1, Brody SL, Ferkol TW, Shoseyov D, Wasserman MG, Ta-shma A, Wilson KS, Bayly PV, Amirav I, Cohen-Cymberknoh M, Dutcher SK, Elpeleg O, Kerem E.
- PloS one.PLoS One.2013 Aug 26;8(8):e72299. doi: 10.1371/journal.pone.0072299. eCollection 2013.
- BACKGROUND: Primary ciliary dyskinesia (PCD) is a genetic disorder characterized by impaired ciliary function, leading to chronic sinopulmonary disease. The genetic causes of PCD are still evolving, while the diagnosis is often dependent on finding a ciliary ultrastructural abnormality and immotile
- PMID 23991085
- Diagnostic testing of patients suspected of primary ciliary dyskinesia.
- Stannard WA1, Chilvers MA, Rutman AR, Williams CD, O'Callaghan C.
- American journal of respiratory and critical care medicine.Am J Respir Crit Care Med.2010 Feb 15;181(4):307-14. doi: 10.1164/rccm.200903-0459OC. Epub 2009 Nov 12.
- RATIONALE: Electron microscopy (EM) of ciliated epithelium is widely used to diagnose primary ciliary dyskinesia (PCD). Ciliary beat frequency (CBF) has been used to screen samples to determine whether EM is indicated. Beat pattern analysis has been advocated as an additional diagnostic test. Neithe
- PMID 19910612
Japanese Journal
- 塩酸クレンブテロールとアジスロマイシンが有効であったimmotile-dyskinetic cilia syndrome の1例
- 伊藤 昌之,岸 厚次,中村 博幸,畑尾 英一,来生 研,須藤 晃彦,小林 克行,土田 文宏,足立 秀喜,柳生 久永,大石 修司,松岡 健
- 日本呼吸器学会雑誌 = The journal of the Japanese Respiratory Society 40(7), 617-621, 2002-07-10
- NAID 10010824003
- 線毛運動不全症候群 (特集 呼吸器疾患の診断・治療の最近の進歩) -- (話題の疾患)
- Dyskihetic cilia syndrome を伴った軟骨形成性気管気管支症の1小児例
- 山岡 光子,吉田 眞,泉 達郎,斎藤 加代子,福山 幸夫,玉置 淳,河上 牧夫,YAMAOKA Mitsuko,YOSHIDA Makoto,IZUMI Tatsuro,SAITO Kayoko,FUKUYAMA Yukio,TAMAOKI Jun,KAWAKAMI Makio
- 東京女子医科大学雑誌 62(11), 1505-1513, 1992-11-25
- NAID 120002360078
Related Links
- 1. Chest. 1980 Oct;78(4):580-2. The dyskinetic cilia syndrome. Ciliary motility in immotile cilia syndrome. Rossman CM, Forrest JB, Lee RM, Newhouse MT. Ciliary motility was studied in three patients with Kartagener ...
- View This Abstract Online The dyskinetic cilia syndrome. Ciliary motility in immotile cilia syndrome. Chest. 1980; 78(4):580-2 (ISSN: 0012-3692) Rossman CM; Forrest JB; Lee RM; Newhouse MT Ciliary motility was ...
★リンクテーブル★
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- 英
- ciliary dyskinesia, dyskinetic cilia syndrome
- 関
- 線毛機能不全、線毛運動不全症、線毛運動障害
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- 関
- dyskinesia、dyskinesis、dysmotility、movement disorder
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