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
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- 1. Lambert-Eaton筋無力症候群の臨床的特徴および診断 clinical features and diagnosis of lambert eaton myasthenic syndrome
- 2. 重症筋無力症の鑑別診断 differential diagnosis of myasthenia gravis
- 3. Lambert-Eaton筋無力症候群の治療 treatment of lambert eaton myasthenic syndrome
- 4. 重症筋無力症患者に対する麻酔 anesthesia for the patient with myasthenia gravis
- 5. 成人におけるギラン・バレー症候群の臨床的特徴および診断 clinical features and diagnosis of guillain barre syndrome in adults
English Journal
- A novel mutation in the TPR6 domain of the RAPSN gene associated with congenital myasthenic syndrome.
- Leshinsky-Silver E, Shapira D, Yosovitz K, Ginsberg M, Lerman-Sagie T, Lev D.SourceMolecular Genetic Laboratory, Wolfson Medical Center, Holon, Israel; Metabolic Neurogenetic Clinic, Wolfson Medical Center, Holon, Israel; Pediatric Neuromuscular Clinic, Wolfson Medical Center, Holon, Israel; Sackler Medical School, Tel Aviv University, Tel Aviv, Israel.
- Journal of the neurological sciences.J Neurol Sci.2012 May 15;316(1-2):112-5. Epub 2012 Feb 10.
- Congenital myasthenic syndromes (CMS) are rare genetic disorders characterized by impaired neuromuscular transmission. They are caused by mutations in synaptic, presynaptic and post synaptic proteins. Rapsyn is a postsynaptic peripheral membrane protein that anchors the nicotinic acetylcholine recep
- PMID 22326364
- SOX1 antibodies in sera from patients with paraneoplastic neurological syndromes.
- Stich O, Klages E, Bischler P, Jarius S, Rasiah C, Voltz R, Rauer S.SourceDepartment of Neurology, Albert Ludwigs University, Freiburg, GermanyDivision of Molecular Neuroimmunology, Department of Neurology, University of Heidelberg, Heidelberg, Germanyravo Diagnostika GmbH, Freiburg, GermanyDepartment of Palliative Medicine, University of Cologne, Cologne, Germany.
- Acta neurologica Scandinavica.Acta Neurol Scand.2012 May;125(5):326-31. doi: 10.1111/j.1600-0404.2011.01572.x. Epub 2011 Jul 14.
- Objectives - SOX1 antibodies have been described in patients with Lambert-Eaton myasthenic syndrome (LEMS) in association with voltage-gated calcium channel antibodies as serological markers of small cell lung cancer (SCLC). This study was aimed to screen for additional SOX1 autoimmunity in onc
- PMID 21751968
Japanese Journal
- 多彩な腫瘍随伴症状を呈した小細胞肺癌の1例
- 若槻 雅敏,松尾 潔,萱谷 紘枝,藤原 慶一,米井 敏郎,佐藤 利雄
- 日本呼吸器学会雑誌 = The journal of the Japanese Respiratory Society 49(7), 517-522, 2011-07-10
- NAID 10029372395
- Lambert-Eaton筋無力症候群 (特集 神経筋接合部--基礎から臨床まで)
- 本村 政勝,福田 卓
- Brain and nerve 63(7), 745-754, 2011-07
- NAID 40018922082
Related Links
- Congenital myasthenic syndrome (CMS) is an inherited neuromuscular disorder caused by defects of several types at the neuromuscular junction. The effects of the disease are similar to Lambert-Eaton syndrome and Myasthenia gravis, the ...
- Lambert–Eaton myasthenic syndrome (LEMS, sometimes Lambert–Eaton syndrome or Eaton–Lambert syndrome) is a rare autoimmune disorder that is characterised by muscle weakness of the limbs. It is the result of an autoimmune reaction, ...
Related Pictures
★リンクテーブル★
「ランバート・イートン症候群」
- 英
- Lambert-Eaton syndrome LES, Lambert-Eaton myasthenic syndrome, LEMS
- 同
- ランバート・イートン筋無力症症候群 Lambert-Eaton筋無力症
- イートン・ランバート症候群 Eaton-Lambert syndrome
- 筋無力症候群 myasthenic syndrome
- 関
- 漸増
病因
- 電位依存性Ca2+チャネルに対する自己抗体
- http://suuchan.net/pukiwiki/pukiwiki.php?Lambert-Eaton%B6%DA%CC%B5%CE%CF%BE%C9
症候
- 四肢近位筋の易疲労性と脱力、腱反射消失。反復刺激により筋力の増加
- 自律神経の障害：性機能低下(勃起不全)、口渇
- 眼症状や球症状が見られることは少ない。
合併症
- 悪性腫瘍(症例の2/3)：その80%以上で肺小細胞癌
検査
- 誘発筋電図：漸増 waxing
- 10Hz以上の高頻度反復刺激により、振幅が漸増していく減少
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国試
参考
- 1. [charged] Clinical features and diagnosis of Lambert-Eaton myasthenic syndrome - uptodate [1]
「congenital myasthenic syndrome」
- 同
- CMS
「slow-channel congenital myasthenic syndrome」
「postsynaptic congenital myasthenic syndrome」
「Lambert-Eaton myasthenic syndrome」
「congenital myasthenic syndromes」
「myasthenic」
- adj.
- 筋無力症の
「syndrome」
- n.