Glanzmann thrombasthenia

出典: meddic

グランツマン血小板無力症

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出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2016/07/04 13:41:08」(JST)

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英文文献

  • Lessons from recurrent deep vein thrombosis in Glanzmann thrombasthenia.
  • Ragsdell B, Thachil J.SourceSchool of Medicine, University of Manchester, Manchester, UK.
  • Haemophilia : the official journal of the World Federation of Hemophilia.Haemophilia.2013 Nov;19(6):e391-3. doi: 10.1111/hae.12261. Epub 2013 Aug 28.
  • PMID 23992524
  • Asymmetrical crying face concomitant with Glanzmann's thrombasthenia.
  • Bay A, Aktekin E, Ergun S, Ozen S.SourceaDivision of Pediatric Hematology, Department of Pediatrics, School of Medicine bDepartment of Pediatrics cDepartment of Medical Biology, Gaziantep University, Gaziantep, Turkey.
  • Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.Blood Coagul Fibrinolysis.2013 Oct 12. [Epub ahead of print]
  • We report a case of a 3-month-old Turkish girl who had clinical and laboratory features of Glanzmann's thrombasthenia associated with asymmetric crying facies (ACF). Although ACF is a minor anomaly, it should not be forgotten that it can be accompanied by major congenital anomalies and if this findi
  • PMID 24126248
  • Procoagulant Platelets Form an α-Granule Protein-covered "Cap" on Their Surface That Promotes Their Attachment to Aggregates.
  • Abaeva AA, Canault M, Kotova YN, Obydennyy SI, Yakimenko AO, Podoplelova NA, Kolyadko VN, Chambost H, Mazurov AV, Ataullakhanov FI, Nurden AT, Alessi MC, Panteleev MA.SourceFrom the Center for Theoretical Problems of Physicochemical Pharmacology, 119991 Moscow, Russia.
  • The Journal of biological chemistry.J Biol Chem.2013 Oct 11;288(41):29621-32. doi: 10.1074/jbc.M113.474163. Epub 2013 Aug 30.
  • Strongly activated "coated" platelets are characterized by increased phosphatidylserine (PS) surface expression, α-granule protein retention, and lack of active integrin αIIbβ3. To study how they are incorporated into thrombi despite a lack of free activated integrin, we investigated the structur
  • PMID 23995838

和文文献

  • Molecular analysis of a patient with type I Glanzmann thrombasthenia and clinical impact of the presence of anti-αIIbβ3 alloantibodies
  • KASHIWAGI Hirokazu,KIYOMIZU Kazunobu,KAMAE Tsuyoshi,NAKAZAWA Tsuyoshi,TADOKORO Seiji,TAKIGUCHI Shuji,DOKI Yuichiro,KANAKURA Yuzuru,TOMIYAMA Yoshiaki
  • International journal of hematology 93(1), 106-111, 2011-01-01
  • NAID 10029532736
  • Acute Epidural Hematoma in a Patient With Glanzmann's Thrombasthenia : Case Report
  • YAMAHATA Hitoshi,HIRAHARA Kazuho,TOMOSUGI Tetsuzo,YAMADA Masahiko,ISHII Takeshi,UETSUHARA Koichi,KAWAKAMI Kiyoshi,ARITA Kazunori
  • Neurologia medico-chirurgica = 神経外科 50(10), 928-930, 2010-10-15
  • … A 7-year-old girl with Glanzmann's thrombasthenia (GT) fell and hit her head against a table. …
  • NAID 10026743268
  • Surgical Treatment of Cecal Cancer in a Patient with Glanzmann's Thrombasthenia : Report of a Case
  • KABASHIMA AKIRA,UEDA NAOYUKI,YONEMURA YUSUKE,MASHINO KOJIRO,FUJII KYUZO,IKEDA TETSUO,TASHIRO HIDEYA,SAKATA HISANOBU
  • Surgery today : the Japanese journal of surgery 39(11), 1002-1005, 2009-11-01
  • NAID 10025555808

関連リンク

Glanzmann thrombasthenia is a genetic platelet disorder in which the platelet have qualitative or quantitative deficiencies of the fibrinogen receptor αIIbβ3. The genes of both of these proteins are on chromosome 17, and 50 ...
Glanzmann disease is a lifelong condition, and there is no cure. You should take special steps to try to avoid bleeding if you have this condition. Anyone with a bleeding disorder should avoid taking aspirin and other ...

関連画像

 / General / Glanzmann's ThrombastheniaGlanzmann Thrombasthenia treatments Glanzmann thrombasthenia - Dental Glanzmann's thrombasthenia associated with Glanzmann's thrombasthenia associated with Glanzmann's thrombasthenia is an


★リンクテーブル★
リンク元グランツマン血小板無力症」「TA
関連記事thrombasthenia

グランツマン血小板無力症」

  [★]

asthenia
Glanzmann thrombasthenia, GT, Glanzmann's thrombasthenia
血小板無力症 thrombasthenia TAGlanzmann血小板無力症栓球無力症
血小板


  • 血小板数が正常にもかかわらず、血小板凝集能低下により出血時間の延長する疾患
  • Gp IIb/IIIaの欠損、機能低下

概念

  • 血小板膜のGpIIb/IIIaの量的・質的異常に起因する血小板凝集能の障害による先天性出血性疾患

病因

遺伝形式

疫学

病変形成&病理

症状

  • 皮膚や粘膜の出血斑

診断

検査

  • 血小板数、血小板形態:正常
  • 出血時間:著明に延長
  • PT、APTT:正常


治療

予後

予防

TA」

  [★]


thrombasthenia」

  [★] 血小板無力症

WordNet   license wordnet

「a rare autosomal recessive disease in which the platelets do not produce clots in the normal way and hemorrhage results」




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